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FDA 510(k)

WOODLYN SLIT LAMP HSSL-EC

K-Number: K841763 · 1984-08-02

ApplicantWoodlyn, Inc.
Decision Date1984-08-02
Product CodeHLI
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

WOODLYN SLIT LAMP HSSL-EC is the device name listed in this FDA 510(k) record. The listed applicant is Woodlyn, Inc.. It received FDA 510(k) clearance on 1984-08-02 under 510(k) number K841763. The device is classified under product code HLI. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WOODLYN SLIT LAMP HSSL-EC?

WOODLYN SLIT LAMP HSSL-EC is a medical device that received FDA 510(k) clearance on 1984-08-02. The listed applicant is Woodlyn, Inc.. The 510(k) number is K841763.

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

WOODLYN SLIT LAMP HSSL-EC received FDA 510(k) clearance on 1984-08-02, under 510(k) number K841763.

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

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 SLIT LAMP HSSL-EC?

The FDA product code for WOODLYN SLIT LAMP HSSL-EC is HLI.

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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: HLI)

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.

K153080RTVue XR OCT Avanti with AngioVue SoftwareOptovue, Inc.K123316HEINE OMEGA 500Heine Optotechnik GmbH & Co. KGK121739IVUE WITH NORMATIVE DATABASEOptovue, Inc.K120057ENVISU SPECTRAL DOMAIN OPHTHALMIC IMAGING SYSTEM (SDOIS)Bioptigen, Inc.K120238RTVUE XR OCTOptovue, Inc.K111531RHA2020Annidis Health Systems Corp.

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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