FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

MKM (MULTIPLE COORDINATE MANIPULATOR) SYSTEM

K Number: K942233 · Decision Jul 1, 1994
Classifications
1
FEI Numbers
72
Registration Numbers
72
Same Product Code
17
Applicant Total
44
Review Days
53

Basic Information

Device Name
MKM (MULTIPLE COORDINATE MANIPULATOR) SYSTEM
K Number
K942233
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4700
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
CARL ZEISS, INC.
Date Received
May 9, 1994
Decision Date
July 1, 1994
Product Code
EPT
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
EPT Microscope, Surgical

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