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

WOODLYN FULL APERTURE TRIAL LENS SET

K Number: K900478 · Decision Feb 21, 1990
Classifications
1
FEI Numbers
56
Registration Numbers
56
Same Product Code
12
Applicant Total
19
Review Days
20

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Basic Information

Device Name
WOODLYN FULL APERTURE TRIAL LENS SET
K Number
K900478
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
886.1405
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Applicant
Woodlyn, Inc.
Date Received
February 1, 1990
Decision Date
February 21, 1990
Product Code
HPC
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
HPC Set, Lens, Trial, Ophthalmic

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Other Clearances by Woodlyn, Inc.

K Number Device Name
K931303 WOODLYN OPERATION MICROSCOPE
K920861 WOODLYN CLASSIC LENSMETER
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. →