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

HUMPHREY OCT SCANNER

K Number: K961171 · Decision Jun 21, 1996
Classifications
1
FEI Numbers
53
Registration Numbers
53
Same Product Code
86
Applicant Total
44
Review Days
88

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
HUMPHREY OCT SCANNER
K Number
K961171
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
886.1570
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Carl Zeiss, Inc.
Date Received
March 25, 1996
Decision Date
June 21, 1996
Product Code
HLI
Advisory Committee
Ophthalmic
Review Advisory Committee
RA
Third Party
N

Classifications

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

Product Code Device Name
HLI Ophthalmoscope, Ac-Powered

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (HLI), ordered by most recent decision date.

View all

Other Clearances by Carl Zeiss, Inc.

K Number Device Name
K013402 VISULAS 532S
K003885 VISULAS YAG II
K993357 IOLMASTER
K983868 OPMI TWINER SURGICAL MICROSCOPE
K965139 SURGICAL MICROSCOPE NAVIGATOR (SMN) SYSTEM/SURGICAL TOOL NAVIGATOR (STN) SYSTEM
K961380 CPC PROBE
K954167 HUMPHREY FIELD ANALYZER (HFA II)
K952894 VISULINK 900 ARGON
K950985 ZEISS ENDOLIVE STERO ENDOSCOPE
K931478 ZEISS OPMI L STEREO-LAPAROSCOPE
Search all 44 clearances from Carl Zeiss, Inc. →