FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

ZIESS ENDOPROBE

K Number: K922735 · Decision Jul 9, 1992
Classifications
1
FEI Numbers
26
Registration Numbers
27
Same Product Code
29
Applicant Total
44
Review Days
31

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Basic Information

Device Name
ZIESS ENDOPROBE
K Number
K922735
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
886.4690
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Carl Zeiss, Inc.
Date Received
June 8, 1992
Decision Date
July 9, 1992
Product Code
HQB
Advisory Committee
Ophthalmic
Review Advisory Committee
OP
Third Party
N

Classifications

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

Product Code Device Name
HQB Photocoagulator And Accessories

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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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