BUCKS NEUROLOGICAL HAMMER
K-Number: K791336 · 1979-08-03
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Device Summary
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
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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