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FDA 510(k)

FINGER MUSCLE TESTER

K-Number: K770164 · 1977-01-28

ApplicantBel-Art Products
Decision Date1977-01-28
Product CodeISD
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

FINGER MUSCLE TESTER is the device name listed in this FDA 510(k) record. The listed applicant is Bel-Art Products. It received FDA 510(k) clearance on 1977-01-28 under 510(k) number K770164. The device is classified under product code ISD. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FINGER MUSCLE TESTER?

FINGER MUSCLE TESTER is a medical device that received FDA 510(k) clearance on 1977-01-28. The listed applicant is Bel-Art Products. The 510(k) number is K770164.

When did FINGER MUSCLE TESTER receive FDA 510(k) clearance?

FINGER MUSCLE TESTER received FDA 510(k) clearance on 1977-01-28, under 510(k) number K770164.

Who is the listed applicant for FINGER MUSCLE TESTER?

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

What is the FDA product code for FINGER MUSCLE TESTER?

The FDA product code for FINGER MUSCLE TESTER is ISD.

Related Clinical Trials

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.

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Other records listing Bel-Art Products 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.

K813524CENTIDISCK770167KNEE SEPARATOR

Related Devices (Code: ISD)

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.

K202979MR Egometer Pedal, MR Ergometer Push/Pull, MR Ergometer Up/Down, MR Ergometer Dorsal Ankle Flex, MR Ergometer Pedal UltraLode B.V.K183296REAL Immersive SystemPenumbra, Inc.K112121ERGOSELECT/GEErgoline GmbHK080545ACTITRAINERActigraph, LLCK053078ERGOSELECT 100 K/P, ERGOSELECT 200 K/PErgoline GmbHK990866QUINTON MEDTRACK CR PLUS TREADMILLQuinton, Inc.

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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