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FDA 510(k)

OPHTHALMIC PROJECTOR

K-Number: K921214 · 1992-06-11

ApplicantLuneau Ophtalmologie SA
Decision Date1992-06-11
Product CodeHOS
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

OPHTHALMIC PROJECTOR is the device name listed in this FDA 510(k) record. The listed applicant is Luneau Ophtalmologie SA. It received FDA 510(k) clearance on 1992-06-11 under 510(k) number K921214. 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 OPHTHALMIC PROJECTOR?

OPHTHALMIC PROJECTOR is a medical device that received FDA 510(k) clearance on 1992-06-11. The listed applicant is Luneau Ophtalmologie SA. The 510(k) number is K921214.

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

OPHTHALMIC PROJECTOR received FDA 510(k) clearance on 1992-06-11, under 510(k) number K921214.

Who is the listed applicant for OPHTHALMIC PROJECTOR?

The FDA 510(k) record lists Luneau Ophtalmologie SA as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for OPHTHALMIC PROJECTOR?

The FDA product code for OPHTHALMIC PROJECTOR is HOS.

Related Clinical Trials

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.

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Other records listing Luneau Ophtalmologie SA 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.

K922253KERATOREF L60K913961OPHTHALMIC STAND

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.K890992WOODLYN OPHTHALMIC PROJECTORWoodlyn, Inc.K862519BAUSCH & LOMB ACCU-CHART 3 ACUITY PROJECTORBausch & Lomb, Inc.K812706MILLER/NADLER GLARE TESTERMosebach Electric & Supply

Official Source

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

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