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FDA 510(k)

BUCKS NEUROLOGICAL HAMMER

K-Number: K791336 · 1979-08-03

Decision Date1979-08-03
Product CodeGWZ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

BUCKS 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 K791336. 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 BUCKS NEUROLOGICAL HAMMER?

BUCKS 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 K791336.

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

BUCKS NEUROLOGICAL HAMMER received FDA 510(k) clearance on 1979-08-03, under 510(k) number K791336.

Who is the listed applicant for BUCKS 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 BUCKS NEUROLOGICAL HAMMER?

The FDA product code for BUCKS NEUROLOGICAL HAMMER is GWZ.

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.

Other records listing Amdia Medical 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.

Related Devices (Code: GWZ)

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.

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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