FDA.reportPublic FDA data

Delta Fly®

Primary DI
08032248369023
Brand
Delta Fly®
Company
DELTA MED SPA
Model
3690222
Device description
Delta Fly Micro Bore F20 Winged Safety Needle
Published
2016-09-23
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
Sterile
true
Single use
true

Product Codes#

Code, Name table
CodeName
FPASet, Administration, Intravascular

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
FPASet, Administration, IntravascularGeneral Hospital2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K140175000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K140175000INTRAVASCULAR ADMINISTRATION SETDelta Med Spa2014-08-05FPA

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
38032248369024PackageGS160In Commercial Distribution
58032248369028PackageGS120In Commercial Distribution
08032248369023PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, EAN-13 table
Source identifierGTIN-14 normalizedEAN-13
3803224836902438032248369024
5803224836902858032248369028
08032248369023080322483690238032248369023

GMDN Terms#

Term, Definition table
TermDefinition
Venous butterfly needle/setAn invasive, hollow, tubular, metal device intended to puncture a vein to collect blood and/or for transient (<24 hours) or short-term (<= 30 days) administration of intravenous (IV) fluids. It includes wings for fixation/placement and may include tubing and/or connectors; however, it does not include accessories to facilitate introduction (e.g., stylet). The device may also be referred to as butterfly needle or scalp vein needle. This is a single-use device.

Device Sizes#

Type, Value, Unit table
TypeValueUnit
Length20Millimeter
Needle Gauge25Gauge
Outer Diameter0.5Millimeter
Pore Size20Micrometer

Regulatory Flags#

DUNS number
444776777
Device count
1
Lot or batch
true
Manufacturing date on label
true
Expiration date on label
true
No natural rubber latex
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
08032248487123AtmosUD-462152025-09-02
08032248487147AtmosUD-A582452025-09-02
08032248487185Infusion SetMMT11732025-09-02
08032248490130AtmosUD-AELN2025-09-02
38032248487124AtmosUD-462152025-09-02
08032248487130AtmosUD-A362052025-09-02
38032248487148AtmosUD-A582452025-09-02
38032248487186Infusion SetMMT11732025-09-02
38032248490131AtmosUD-AELN2025-09-02
08032248471030Securmeter Foley ManometerHM0042025-05-19
38032248471031Securmeter Foley ManometerHM0042025-05-19
08032248127401NA12T74002016-09-23
08032248007123SOL CARE T SIV0012021-03-30
08032248007130SOL CARE T SIV0022021-03-30
08032248007147SOL CARE T SIV0032021-03-30
08032248007154SOL CARE T SIV0042021-03-30
08032248007161SOL CARE T SIV0052021-03-30
08032248007178SOL CARE T SIV0062021-03-30
08032248007185SOL CARE T SIV0072021-03-30
08032248007192SOL CARE T SIV0082021-03-30

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05051684018503LifeportAngiodynamics, Inc.FPA2026-06-23
05051684018510LifeportAngiodynamics, Inc.FPA2026-06-23
05051684018527LifeportAngiodynamics, Inc.FPA2026-06-23
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05051684018589LifeguardAngiodynamics, Inc.FPA2026-06-23
05051684018596LifeguardAngiodynamics, Inc.FPA2026-06-23
05051684018602LifeguardAngiodynamics, Inc.FPA2026-06-23
05051684018619LifeguardAngiodynamics, Inc.FPA2026-06-23
05051684018626LifeguardAngiodynamics, Inc.FPA2026-06-23
05051684018633LifeguardAngiodynamics, Inc.FPA2026-06-23
05051684018640LifeguardAngiodynamics, Inc.FPA2026-06-23
00811505030573IvenixFresenius Kabi AGFPA2026-06-02
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00085412676630DUO-VENTBAXTER HEALTHCARE CORPORATIONFPA2023-07-11
00634624911109Precision Delivery Bifurcated IV Extension SetQUEST MEDICAL INCFPA2022-12-19
00634624911048High-Flow Extension SetQUEST MEDICAL INCFPA2022-12-12
00634624101159Q2 IV Administration SetQUEST MEDICAL INCFPA2022-12-06