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

WOODLYN CLASSIC LENSMETER

K Number: K920861 · Decision Jul 30, 1992
Classifications
1
FEI Numbers
64
Registration Numbers
65
Same Product Code
15
Applicant Total
19
Review Days
156

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
WOODLYN CLASSIC LENSMETER
K Number
K920861
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
886.1425
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Woodlyn, Inc.
Date Received
February 25, 1992
Decision Date
July 30, 1992
Product Code
HLM
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
HLM Instrument, Measuring, Lens, Ac-Powered

Similar 510(k) Clearances

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

View all

Other Clearances by Woodlyn, Inc.

K Number Device Name
K931303 WOODLYN OPERATION MICROSCOPE
K900478 WOODLYN FULL APERTURE TRIAL LENS SET
K900476 WOODLYN SLIT LAMP MODEL HR-1
K900477 WOODLYN CLASSIC SLIT LAMP MODEL SMM
K890992 WOODLYN OPHTHALMIC PROJECTOR
K874900 WOODLYN CLASSIC REFRACTOR, PHOROPTOR
K843812 WOODLYN CLASSIC CATARACT ACUITY TEST
K841761 WOODLYN CLASSIC SLIT LAMP HSSL-CL
K841765 WOODLYN STANDARD SLIT LAMP HSSL-ST
K841767 WOODLYN CLASSIC KERATOMETER
Search all 19 clearances from Woodlyn, Inc. →