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FDA 510(k)

WOODLYN CLASSIC LENSMETER

K-Number: K920861 · 1992-07-30

ApplicantWoodlyn, Inc.
Decision Date1992-07-30
Product CodeHLM
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

WOODLYN CLASSIC LENSMETER is the device name listed in this FDA 510(k) record. The listed applicant is Woodlyn, Inc.. It received FDA 510(k) clearance on 1992-07-30 under 510(k) number K920861. The device is classified under product code HLM. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WOODLYN CLASSIC LENSMETER?

WOODLYN CLASSIC LENSMETER is a medical device that received FDA 510(k) clearance on 1992-07-30. The listed applicant is Woodlyn, Inc.. The 510(k) number is K920861.

When did WOODLYN CLASSIC LENSMETER receive FDA 510(k) clearance?

WOODLYN CLASSIC LENSMETER received FDA 510(k) clearance on 1992-07-30, under 510(k) number K920861.

Who is the listed applicant for WOODLYN CLASSIC LENSMETER?

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 CLASSIC LENSMETER?

The FDA product code for WOODLYN CLASSIC LENSMETER is HLM.

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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 MICROSCOPEK900478WOODLYN FULL APERTURE TRIAL LENS SETK900477WOODLYN CLASSIC SLIT LAMP MODEL SMMK900476WOODLYN SLIT LAMP MODEL HR-1K890992WOODLYN OPHTHALMIC PROJECTORK874900WOODLYN CLASSIC REFRACTOR, PHOROPTOR

View all 19 devices →

Related Devices (Code: HLM)

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.

K944022LENSCHEKLeica, Inc.K940997AL-3300Hoya Corp. USAK936199AUTOMATIC LENSOMETERCanon USA, Inc.K930441MARCO STANDARD LENSMETERS 101,201Marco Ophthalmic, Inc.K930445MARCO LM-770 DIGITAL PROJECTION LENSMETERMarco Ophthalmic, Inc.K924785BURTON RADIUSGAUGE - MODEL 2030R.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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