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FDA 510(k)

WOODLYN SLIT LAMP MODEL HR-1

K-Number: K900476 · 1990-02-21

ApplicantWoodlyn, Inc.
Decision Date1990-02-21
Product CodeHJO
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

WOODLYN SLIT LAMP MODEL HR-1 is the device name listed in this FDA 510(k) record. The listed applicant is Woodlyn, Inc.. It received FDA 510(k) clearance on 1990-02-21 under 510(k) number K900476. The device is classified under product code HJO. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WOODLYN SLIT LAMP MODEL HR-1?

WOODLYN SLIT LAMP MODEL HR-1 is a medical device that received FDA 510(k) clearance on 1990-02-21. The listed applicant is Woodlyn, Inc.. The 510(k) number is K900476.

When did WOODLYN SLIT LAMP MODEL HR-1 receive FDA 510(k) clearance?

WOODLYN SLIT LAMP MODEL HR-1 received FDA 510(k) clearance on 1990-02-21, under 510(k) number K900476.

Who is the listed applicant for WOODLYN SLIT LAMP MODEL HR-1?

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 MODEL HR-1?

The FDA product code for WOODLYN SLIT LAMP MODEL HR-1 is HJO.

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.

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.

View all 19 devices →

Related Devices (Code: HJO)

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.

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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