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FDA 510(k)

OPHTHALMIC TABLE

K-Number: K841759 · 1984-06-01

ApplicantWoodlyn, Inc.
Decision Date1984-06-01
Product CodeHMG
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

OPHTHALMIC TABLE is the device name listed in this FDA 510(k) record. The listed applicant is Woodlyn, Inc.. It received FDA 510(k) clearance on 1984-06-01 under 510(k) number K841759. The device is classified under product code HMG. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OPHTHALMIC TABLE?

OPHTHALMIC TABLE is a medical device that received FDA 510(k) clearance on 1984-06-01. The listed applicant is Woodlyn, Inc.. The 510(k) number is K841759.

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

OPHTHALMIC TABLE received FDA 510(k) clearance on 1984-06-01, under 510(k) number K841759.

Who is the listed applicant for OPHTHALMIC TABLE?

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 OPHTHALMIC TABLE?

The FDA product code for OPHTHALMIC TABLE is HMG.

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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 LENSMETERK900478WOODLYN FULL APERTURE TRIAL LENS SETK900476WOODLYN SLIT LAMP MODEL HR-1K900477WOODLYN CLASSIC SLIT LAMP MODEL SMMK890992WOODLYN OPHTHALMIC PROJECTOR

View all 19 devices →

Related Devices (Code: HMG)

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.

K900161A-SCAN ROLL-AROUND STANDJedmed Instrument Co.K883575MODIFIED SITE MOBILE STAND FOR OPHTHALMIC USESite Microsurgical Systems, Inc.K873554GORSK INSTRUMENT RESTGorsk, Inc.

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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