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FDA 510(k)

WOODLYN STANDARD SLIT LAMP HSSL-ST

K-Number: K841765 · 1984-08-07

ApplicantWoodlyn, Inc.
Decision Date1984-08-07
Product CodeHLQ
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

WOODLYN STANDARD SLIT LAMP HSSL-ST is the device name listed in this FDA 510(k) record. The listed applicant is Woodlyn, Inc.. It received FDA 510(k) clearance on 1984-08-07 under 510(k) number K841765. The device is classified under product code HLQ. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WOODLYN STANDARD SLIT LAMP HSSL-ST?

WOODLYN STANDARD SLIT LAMP HSSL-ST is a medical device that received FDA 510(k) clearance on 1984-08-07. The listed applicant is Woodlyn, Inc.. The 510(k) number is K841765.

When did WOODLYN STANDARD SLIT LAMP HSSL-ST receive FDA 510(k) clearance?

WOODLYN STANDARD SLIT LAMP HSSL-ST received FDA 510(k) clearance on 1984-08-07, under 510(k) number K841765.

Who is the listed applicant for WOODLYN STANDARD SLIT LAMP HSSL-ST?

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 STANDARD SLIT LAMP HSSL-ST?

The FDA product code for WOODLYN STANDARD SLIT LAMP HSSL-ST is HLQ.

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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

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Related Devices (Code: HLQ)

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.

K003299OPD-SCAN, MODELS ARK-10000 AND ARK-9000Nidek Co., Ltd.K973756EYE SYS VISTAEyesys Technologies, Inc.K964290EYECHEKReichert Ophthalmic Instruments, Div. Leica, Inc.K945382TECHNOMED C-SCAN COLOR ELLIPSOID TOPOMETERExpertech Assoc., Inc.K944207TOPOGRAPHIC MODELING SYSTEM 2 TMS-2Computed Anatomy, Inc.K944616KERATRON CORNEAL TOPOGRAPHERAlliance Medical Marketinig

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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