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

IOLMASTER

K Number: K993357 · Decision Mar 20, 2000
Classifications
1
FEI Numbers
54
Registration Numbers
55
Same Product Code
107
Applicant Total
44
Review Days
166

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Basic Information

Device Name
IOLMASTER
K Number
K993357
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
886.1850
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Carl Zeiss, Inc.
Date Received
October 6, 1999
Decision Date
March 20, 2000
Product Code
HJO
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
HJO Biomicroscope, Slit-Lamp, Ac-Powered

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K961380 CPC PROBE
K961171 HUMPHREY OCT SCANNER
K954167 HUMPHREY FIELD ANALYZER (HFA II)
K952894 VISULINK 900 ARGON
K950985 ZEISS ENDOLIVE STERO ENDOSCOPE
K931478 ZEISS OPMI L STEREO-LAPAROSCOPE
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