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FDA 510(k)

WOODLYN FULL APERTURE TRIAL LENS SET

K-Number: K900478 · 1990-02-21

ApplicantWoodlyn, Inc.
Decision Date1990-02-21
Product CodeHPC
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

WOODLYN FULL APERTURE TRIAL LENS SET is the device name listed in this FDA 510(k) record. The listed applicant is Woodlyn, Inc.. It received FDA 510(k) clearance on 1990-02-21 under 510(k) number K900478. The device is classified under product code HPC. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WOODLYN FULL APERTURE TRIAL LENS SET?

WOODLYN FULL APERTURE TRIAL LENS SET is a medical device that received FDA 510(k) clearance on 1990-02-21. The listed applicant is Woodlyn, Inc.. The 510(k) number is K900478.

When did WOODLYN FULL APERTURE TRIAL LENS SET receive FDA 510(k) clearance?

WOODLYN FULL APERTURE TRIAL LENS SET received FDA 510(k) clearance on 1990-02-21, under 510(k) number K900478.

Who is the listed applicant for WOODLYN FULL APERTURE TRIAL LENS SET?

The FDA 510(k) record lists Woodlyn, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for WOODLYN FULL APERTURE TRIAL LENS SET?

The FDA product code for WOODLYN FULL APERTURE TRIAL LENS SET is HPC.

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Other records listing Woodlyn, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K931303WOODLYN OPERATION MICROSCOPEK920861WOODLYN CLASSIC LENSMETERK900476WOODLYN SLIT LAMP MODEL HR-1K900477WOODLYN CLASSIC SLIT LAMP MODEL SMMK890992WOODLYN OPHTHALMIC PROJECTORK874900WOODLYN CLASSIC REFRACTOR, PHOROPTOR

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Related Devices (Code: HPC)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K945443BOBES LENS SETBobes S.A.K951437OTI MODEL TLS-60Oti Medical, LLCK930195OPHTHALMIC TRIAL LENSESOptimark Accessories and InstrumentsK934859CONTACT LENSESArno Intl., Inc.K930446MARCO TRIAL SETSMarco Ophthalmic, Inc.K924786BURTON TRIAL LENS SETR.H. Burton Co.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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