FDA 510(k)

TAYLOR NEUROLOGICAL HAMMER

K-Number: K791337 · 1979-08-03

Decision Date1979-08-03

Product CodeGWZ

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

TAYLOR NEUROLOGICAL HAMMER is the device name listed in this FDA 510(k) record. The listed applicant is Amdia Medical Products. It received FDA 510(k) clearance on 1979-08-03 under 510(k) number K791337. The device is classified under product code GWZ. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TAYLOR NEUROLOGICAL HAMMER?

TAYLOR NEUROLOGICAL HAMMER is a medical device that received FDA 510(k) clearance on 1979-08-03. The listed applicant is Amdia Medical Products. The 510(k) number is K791337.

When did TAYLOR NEUROLOGICAL HAMMER receive FDA 510(k) clearance?

TAYLOR NEUROLOGICAL HAMMER received FDA 510(k) clearance on 1979-08-03, under 510(k) number K791337.

Who is the listed applicant for TAYLOR NEUROLOGICAL HAMMER?

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

What is the FDA product code for TAYLOR NEUROLOGICAL HAMMER?

The FDA product code for TAYLOR NEUROLOGICAL HAMMER is GWZ.

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Other records listing Amdia Medical Products as applicant

K791334MULTISCOPE K791333BOWLES STETHOSCOPE K791335NURSESCOPE K791338DUAL HEAD STETHOSCOPE K791336BUCKS NEUROLOGICAL HAMMER

Related Devices (Code: GWZ)

K891571PERCUSSION HAMMERSandal Surgico K852716TAYLOR PERCUSSION HAMMER SS 410 OR 420The Huxley Instrument Corp.K8517481/310, 1-320 PERCUSSION HAMMERS,TAYLOR, DEJERINEArtiberia K834170OP-CON SURG. INSTRUMENT #10Imm Enterprises , Ltd.K840314CAT 10-NEUROLOGY DEVICEImm Enterprises , Ltd.K834178H.R. JAKOBI SURG. INSTR. #10 34/36Imm Enterprises , Ltd.

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.