BUCKS NEUROLOGICAL HAMMER— 510(k) K791336

Name: FDA 510(k) clearance K791336
Creator: U.S. Food and Drug Administration
Published: 1979-08-03

Substantially Equivalent

Amdia Medical Products

FDA 510(k) clearance K791336 for BUCKS NEUROLOGICAL HAMMER, Substantially Equivalent on 1979-08-03. Applicant: Amdia Medical Products. Device class: 1.

Clearance details

Applicant: Amdia Medical Products
Product code: Code GWZ
Device class: Class 1
Regulation: 21 CFR 882.1700
Advisory panel: Neurology
Date received: 1979-07-20
Decision date: 1979-08-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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K791333 — BOWLES STETHOSCOPE1979-08-10
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K791338 — DUAL HEAD STETHOSCOPE1979-08-10
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