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FDA 510(k)

WOODLYN OPHTHALMIC PROJECTOR

K-Number: K890992 · 1989-05-17

ApplicantWoodlyn, Inc.
Decision Date1989-05-17
Product CodeHOS
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

WOODLYN OPHTHALMIC PROJECTOR is the device name listed in this FDA 510(k) record. The listed applicant is Woodlyn, Inc.. It received FDA 510(k) clearance on 1989-05-17 under 510(k) number K890992. The device is classified under product code HOS. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WOODLYN OPHTHALMIC PROJECTOR?

WOODLYN OPHTHALMIC PROJECTOR is a medical device that received FDA 510(k) clearance on 1989-05-17. The listed applicant is Woodlyn, Inc.. The 510(k) number is K890992.

When did WOODLYN OPHTHALMIC PROJECTOR receive FDA 510(k) clearance?

WOODLYN OPHTHALMIC PROJECTOR received FDA 510(k) clearance on 1989-05-17, under 510(k) number K890992.

Who is the listed applicant for WOODLYN OPHTHALMIC PROJECTOR?

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 OPHTHALMIC PROJECTOR?

The FDA product code for WOODLYN OPHTHALMIC PROJECTOR is HOS.

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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 SMMK900478WOODLYN FULL APERTURE TRIAL LENS SETK874900WOODLYN CLASSIC REFRACTOR, PHOROPTOR

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Related Devices (Code: HOS)

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.

K936200WIRELESS CHART PROJECTOR,HCP-W 721Canon USA, Inc.K930443MARCO CP-600 AUTO CHART PROJECTOR/CP-1 CHART PROJEMarco Ophthalmic, Inc.K924784BURTON PROJECTOR HEAD - MODEL 6000-HR.H. Burton Co.K921214OPHTHALMIC PROJECTORLuneau Ophtalmologie SAK862519BAUSCH & LOMB ACCU-CHART 3 ACUITY PROJECTORBausch & Lomb, Inc.K812706MILLER/NADLER GLARE TESTERMosebach Electric & Supply

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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