MANUAL SURGICAL INSTRUMENTS— 510(k) K920263

Name: FDA 510(k) clearance K920263
Creator: U.S. Food and Drug Administration
Published: 1992-05-06

Substantially Equivalent

Phoenix Instruments Div.

FDA 510(k) clearance K920263 for MANUAL SURGICAL INSTRUMENTS, Substantially Equivalent on 1992-05-06. Applicant: Phoenix Instruments Div.. Device class: 1.

Clearance details

Applicant: Phoenix Instruments Div.
Product code: Code KDC
Device class: Class 1
Regulation: 21 CFR 878.4800
Advisory panel: General, Plastic Surgery
Date received: 1992-01-21
Decision date: 1992-05-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Addison, IL, US

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