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

ZEISS OPERATING KERATOMETER

K Number: K853723 · Decision Oct 15, 1985
Classifications
1
FEI Numbers
17
Registration Numbers
18
Same Product Code
28
Applicant Total
44
Review Days
40

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Basic Information

Device Name
ZEISS OPERATING KERATOMETER
K Number
K853723
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
886.1350
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Applicant
Carl Zeiss, Inc.
Date Received
September 5, 1985
Decision Date
October 15, 1985
Product Code
HLQ
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
HLQ Keratoscope, 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
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