WOODLYN APPLANATION TONOMETER
K-Number: K841762 · 1984-08-02
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Device Summary
Frequently Asked Questions
What is the WOODLYN APPLANATION TONOMETER?
WOODLYN APPLANATION TONOMETER 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 K841762.
When did WOODLYN APPLANATION TONOMETER receive FDA 510(k) clearance?
WOODLYN APPLANATION TONOMETER received FDA 510(k) clearance on 1984-08-02, under 510(k) number K841762.
Who is the listed applicant for WOODLYN APPLANATION TONOMETER?
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 APPLANATION TONOMETER?
The FDA product code for WOODLYN APPLANATION TONOMETER is HKX.
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: HKX)
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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