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FDA 510(k)

MODEL 860-1 VERI/PROBE

K-Number: K820651 · 1982-04-29

ApplicantVerite
Decision Date1982-04-29
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

MODEL 860-1 VERI/PROBE is the device name listed in this FDA 510(k) record. The listed applicant is Verite. It received FDA 510(k) clearance on 1982-04-29 under 510(k) number K820651. 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 MODEL 860-1 VERI/PROBE?

MODEL 860-1 VERI/PROBE is a medical device that received FDA 510(k) clearance on 1982-04-29. The listed applicant is Verite. The 510(k) number is K820651.

When did MODEL 860-1 VERI/PROBE receive FDA 510(k) clearance?

MODEL 860-1 VERI/PROBE received FDA 510(k) clearance on 1982-04-29, under 510(k) number K820651.

Who is the listed applicant for MODEL 860-1 VERI/PROBE?

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 MODEL 860-1 VERI/PROBE?

The FDA product code for MODEL 860-1 VERI/PROBE 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 & POK822929VERIL/PPR PERSONAL PAIN RELIEVER #800K813108MODEL 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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