MKM (MULTIPLE COORDINATE MANIPULATOR) SYSTEM— 510(k) K942233

Name: FDA 510(k) clearance K942233
Creator: U.S. Food and Drug Administration
Published: 1994-07-01

Substantially Equivalent

Carl Zeiss, Inc.

FDA 510(k) clearance K942233 for MKM (MULTIPLE COORDINATE MANIPULATOR) SYSTEM, Substantially Equivalent on 1994-07-01. Applicant: Carl Zeiss, Inc.. Device class: 1.

Clearance details

Applicant: Carl Zeiss, Inc.
Product code: Code EPT
Device class: Class 1
Regulation: 21 CFR 878.4700
Advisory panel: General, Plastic Surgery
Date received: 1994-05-09
Decision date: 1994-07-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Thornwood, NY, US

Download summary PDF View on FDA.gov ↗

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