FDA 510(k)

VERI-FIER

K-Number: K811351 · 1981-07-30

ApplicantVerite

Decision Date1981-07-30

Product CodeGZJ

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

VERI-FIER is the device name listed in this FDA 510(k) record. The listed applicant is Verite. It received FDA 510(k) clearance on 1981-07-30 under 510(k) number K811351. 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 VERI-FIER?

VERI-FIER is a medical device that received FDA 510(k) clearance on 1981-07-30. The listed applicant is Verite. The 510(k) number is K811351.

When did VERI-FIER receive FDA 510(k) clearance?

VERI-FIER received FDA 510(k) clearance on 1981-07-30, under 510(k) number K811351.

Who is the listed applicant for VERI-FIER?

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 VERI-FIER?

The FDA product code for VERI-FIER is GZJ.

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 1000 K840099MODEL 800-A VERI/PPR K840098MODEL 811 VERI/TENS & PO K822929VERIL/PPR PERSONAL PAIN RELIEVER #800 K820651MODEL 860-1 VERI/PROBE K813108MODEL 500 VERI/500

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Related Devices (Code: GZJ)

K252712STIMPOD NMS460 Nerve StimulatorAlgiamed Technologies USA, Inc.K252767actiTENS miniSublimed K252236CP Relief Wand Rx - TENS/NMESN & C Holdings, LLC K232441Unipro (K-UNIPRO-US)Tenscare, Ltd.K241228TENSWaveZynex Medical Officer K233046Electrical 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.