FDA.reportPublic FDA data

Starboard Temperature Probes

Primary DI
10850933007082
Brand
Starboard Temperature Probes
Company
STARBOARD MEDICAL, INC.
Model
400-SK
Catalog number
400-SK
Device description
Skin Temperature Sensor (400 Series Thermistor)
Published
2016-09-30
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
OTC
false
Sterile
true
Single use
true

Product Codes#

Code, Name table
CodeName
FLLThermometer, Electronic, Clinical

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
FLLContinuous Measurement ThermometerGeneral Hospital2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K111282000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K111282000DISPOSABLE TEMPERATURE PROBES / SENSORS AND INTERCONNECT INSTRUMENT CABLESStarboard Medical, LLC2011-08-11FLL

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
10850933007082PackageGS150In Commercial Distribution
00850933007085PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
1085093300708210850933007082
00850933007085008509330070858509330070850850933007085

GMDN Terms#

Term, Definition table
TermDefinition
General-purpose patient temperature probe, single-useA temperature sensing device intended to be placed into a body orifice or on the body surface, and used in conjunction with a separate parent device with a display (e.g., electronic patient thermometer, infant warmer) to enable measurement/monitoring of a patient’s temperature; its use is not dedicated to a specific type of procedure. It is typically constructed of flexible materials (e.g., plastic or rubber) with a metal conducting core; the distal end of different device types will be designed for a particular application site. This is a single-use device.

Sterilization Methods#

Method table
Method

Regulatory Flags#

DUNS number
012983893
Device count
1
DM exempt
false
Premarket exempt
false
HCT/P
false
Kit
false
Combination product
false
Lot or batch
true
Serial number
false
Manufacturing date on label
true
Expiration date on label
true
Donation ID number
false
Contains natural rubber latex
false
No natural rubber latex
true
Sterilization required before use
false

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00850933007009Clik-FIXWCS-1061WCS-10612017-01-30
00850933007016Clik-FIXPCS-1011PCS-10112016-09-30
00850933007139Clik-FIXWCS-1003WCS-10032016-09-30
00850933007146Clik-FIXWCS-1051WCS-10512017-01-30
00850933007184Clik-FIXPCS-1012PCS-10122017-03-16
00850933007191Clik-FIXWCS-1052WCS-10522017-08-07
00850933007221Clik-FIXWCS-1006WCS-10062018-05-30
00866896000018Clik-FIXWCS-1000WCS-10002017-01-24
00850933007269Clik-FIXNPS-1006NPS-10062019-04-18
00850933007153Clik-FIXLLS-1021LLS-10212017-02-27
00850933007160Clik-FIXABS-1022ABS-10222017-03-14
00850933007252Clik-FIXLLS-1024LLS-10242018-10-10
10850933007204Clik-FIXLLSK-1024LLSK-10242019-03-08
20850933007201Clik-FIXLLSK-1024LLSK-10242019-03-08
10850933007242Clik-FIXPCK-1011PCK-10112019-03-08
10850933007006Clik-FIXWCS-1061WCS-10612017-01-30
10850933007013Clik-FIXPCS-1011PCS-10112016-09-30
10850933007136Clik-FIXWCS-1003WCS-10032016-09-30
10850933007143Clik-FIXWCS-1051WCS-10512017-01-30
10850933007181Clik-FIXPCS-1012PCS-10122017-03-16

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Primary DI, Brand, Company table
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00850086928039SENSINEL™ CARDIOPULMONARY MANAGEMENT (CPM) SYSTEM)Analog Devices, Inc.FLL2026-06-03
08720256776567Corsano CardioWatch 287-2 SystemCorsano Health B.V.FLL2026-06-02
06926347900459joybabeShenzhen Brav Electronic Technologies Co., Ltd.FLL2026-06-01
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00884392020613Safety 1stDOREL JUVENILE GROUP, INC.FLL2026-05-28
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