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FDA 510(k)

VERI/CTGS MODEL 850

K-Number: K771122 · 1977-08-04

ApplicantVerite Scientific, Inc.
Decision Date1977-08-04
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

VERI/CTGS MODEL 850 is the device name listed in this FDA 510(k) record. The listed applicant is Verite Scientific, Inc.. It received FDA 510(k) clearance on 1977-08-04 under 510(k) number K771122. 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/CTGS MODEL 850?

VERI/CTGS MODEL 850 is a medical device that received FDA 510(k) clearance on 1977-08-04. The listed applicant is Verite Scientific, Inc.. The 510(k) number is K771122.

When did VERI/CTGS MODEL 850 receive FDA 510(k) clearance?

VERI/CTGS MODEL 850 received FDA 510(k) clearance on 1977-08-04, under 510(k) number K771122.

Who is the listed applicant for VERI/CTGS MODEL 850?

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

What is the FDA product code for VERI/CTGS MODEL 850?

The FDA product code for VERI/CTGS MODEL 850 is GZJ.

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Other records listing Verite Scientific, Inc. 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.

K770323VERI/TRODES

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

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

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