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

S 22 INSTRUMENT STAND

K Number: K891584 · Decision Jun 8, 1989
Classifications
1
FEI Numbers
59
Registration Numbers
59
Same Product Code
13
Applicant Total
44
Review Days
80

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Basic Information

Device Name
S 22 INSTRUMENT STAND
K Number
K891584
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4700
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Carl Zeiss, Inc.
Date Received
March 20, 1989
Decision Date
June 8, 1989
Product Code
HRM
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
HRM Microscope, Operating & Accessories, Ac-Powered, Ophthalmic

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K965139 SURGICAL MICROSCOPE NAVIGATOR (SMN) SYSTEM/SURGICAL TOOL NAVIGATOR (STN) SYSTEM
K961380 CPC PROBE
K961171 HUMPHREY OCT SCANNER
K954167 HUMPHREY FIELD ANALYZER (HFA II)
K952894 VISULINK 900 ARGON
K950985 ZEISS ENDOLIVE STERO ENDOSCOPE
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