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FDA 510(k)

VERIL/PPR PERSONAL PAIN RELIEVER #800

K-Number: K822929 · 1982-11-17

ApplicantVerite
Decision Date1982-11-17
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

VERIL/PPR PERSONAL PAIN RELIEVER #800 is the device name listed in this FDA 510(k) record. The listed applicant is Verite. It received FDA 510(k) clearance on 1982-11-17 under 510(k) number K822929. The device is classified under product code GZJ. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VERIL/PPR PERSONAL PAIN RELIEVER #800?

VERIL/PPR PERSONAL PAIN RELIEVER #800 is a medical device that received FDA 510(k) clearance on 1982-11-17. The listed applicant is Verite. The 510(k) number is K822929.

When did VERIL/PPR PERSONAL PAIN RELIEVER #800 receive FDA 510(k) clearance?

VERIL/PPR PERSONAL PAIN RELIEVER #800 received FDA 510(k) clearance on 1982-11-17, under 510(k) number K822929.

Who is the listed applicant for VERIL/PPR PERSONAL PAIN RELIEVER #800?

The FDA 510(k) record lists Verite as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VERIL/PPR PERSONAL PAIN RELIEVER #800?

The FDA product code for VERIL/PPR PERSONAL PAIN RELIEVER #800 is GZJ.

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Other records listing Verite as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K844727MODEL 1000K840099MODEL 800-A VERI/PPRK840098MODEL 811 VERI/TENS & POK820651MODEL 860-1 VERI/PROBEK813108MODEL 500 VERI/500K813515VERI/DFS TM #817

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Related Devices (Code: GZJ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K252712STIMPOD NMS460 Nerve StimulatorAlgiamed Technologies USA, Inc.K252767actiTENS miniSublimedK252236CP Relief Wand Rx - TENS/NMESN & C Holdings, LLCK232441Unipro (K-UNIPRO-US)Tenscare, Ltd.K241228TENSWaveZynex Medical OfficerK233046Electrical Neuromuscular Stimulator, Cure TrioOriental Inspiration Limited

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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