WOODLYN CLASSIC SLIT LAMP MODEL SMM
K-Number: K900477 · 1990-02-21
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Device Summary
Frequently Asked Questions
What is the WOODLYN CLASSIC SLIT LAMP MODEL SMM?
WOODLYN CLASSIC SLIT LAMP MODEL SMM 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 K900477.
When did WOODLYN CLASSIC SLIT LAMP MODEL SMM receive FDA 510(k) clearance?
WOODLYN CLASSIC SLIT LAMP MODEL SMM received FDA 510(k) clearance on 1990-02-21, under 510(k) number K900477.
Who is the listed applicant for WOODLYN CLASSIC SLIT LAMP MODEL SMM?
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 SLIT LAMP MODEL SMM?
The FDA product code for WOODLYN CLASSIC SLIT LAMP MODEL SMM 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.
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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