CONPHAR PERCUSSION HAMMER(BUCK TYPE)— 510(k) K803174

Name: FDA 510(k) clearance K803174
Creator: U.S. Food and Drug Administration
Published: 1980-12-30

Substantially Equivalent

Conphar, Inc.

FDA 510(k) clearance K803174 for CONPHAR PERCUSSION HAMMER(BUCK TYPE), Substantially Equivalent on 1980-12-30. Applicant: Conphar, Inc.. Device class: 1.

Clearance details

Applicant: Conphar, Inc.
Product code: Code GWZ
Device class: Class 1
Regulation: 21 CFR 882.1700
Advisory panel: Neurology
Date received: 1980-12-15
Decision date: 1980-12-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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