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FDA 510(k)

ADVANCED MEDICAL PRODUCTS MES TENS

K-Number: K852838 · 1985-08-28

ApplicantAdvanced Medical Products, Inc.
Decision Date1985-08-28
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

ADVANCED MEDICAL PRODUCTS MES TENS is the device name listed in this FDA 510(k) record. The listed applicant is Advanced Medical Products, Inc.. It received FDA 510(k) clearance on 1985-08-28 under 510(k) number K852838. 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 ADVANCED MEDICAL PRODUCTS MES TENS?

ADVANCED MEDICAL PRODUCTS MES TENS is a medical device that received FDA 510(k) clearance on 1985-08-28. The listed applicant is Advanced Medical Products, Inc.. The 510(k) number is K852838.

When did ADVANCED MEDICAL PRODUCTS MES TENS receive FDA 510(k) clearance?

ADVANCED MEDICAL PRODUCTS MES TENS received FDA 510(k) clearance on 1985-08-28, under 510(k) number K852838.

Who is the listed applicant for ADVANCED MEDICAL PRODUCTS MES TENS?

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

What is the FDA product code for ADVANCED MEDICAL PRODUCTS MES TENS?

The FDA product code for ADVANCED MEDICAL PRODUCTS MES TENS is GZJ.

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Other records listing Advanced Medical Products, Inc. as applicant

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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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