PainAway Pro

Primary DI
00822383549415
Brand
PainAway Pro
Company
Drive Devilbiss Healthcare
Model
RTLAGF-920
Device description
BackSzLong-Last Elctrde,RTLAGF-900
Published
2016-07-01
Public version status
Update
Distribution status
Not in Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
OTC
true

Product Codes#

Code, Name table
CodeName
NGXSTIMULATOR, MUSCLE, POWERED, FOR MUSCLE CONDITIONING
NUHSTIMULATOR, NERVE, TRANSCUTANEOUS, OVER-THE-COUNTER

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
NGXStimulator, Muscle, Powered, For Muscle ConditioningPhysical Medicine2
NUHStimulator, Nerve, Transcutaneous, Over-The-CounterNeurology2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K102598000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K102598000HI-DOW-XPHi-Dow International, Inc.2011-05-13NUH

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
10822383549412PackageGS150Not in Commercial Distribution
50822383549410PackageGS18Not in Commercial Distribution
00822383549415PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
1082238354941210822383549412
5082238354941050822383549410
00822383549415008223835494158223835494150822383549415

GMDN Terms#

Term, Definition table
TermDefinition
Transcutaneous electrical stimulation leadA non-sterile, insulated, electrical conducting wire intended to be used to connect a transcutaneous electrical stimulation electrode to an electrical stimulus generator (e.g., TENS system generator), or a wire having a distal end that splits and terminates as electrodes which are placed on the patient for the transmission of electrical stimulation. This is a reusable device.

Regulatory Flags#

DUNS number
867673159
Device count
1
Lot or batch
true
Serial number
true

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