Woodlyn Applanation Tonometer

FDA 510(k) K841762 · Woodlyn, Inc.

Substantially Equivalent

510(k) numberK841762

Submission

Device name
Woodlyn Applanation Tonometer
Applicant
Woodlyn, Inc.
Mchenry, IL, US
Received
April 27, 1984
Decision date
August 2, 1984
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
HKX – Tonometer, Ac-Powered
Device class
Class II (moderate risk)
Regulation
21 CFR 886.1930
Specialty
Ophthalmic

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Questions and answers

When was Woodlyn Applanation Tonometer cleared by the FDA?

Woodlyn Applanation Tonometer (K841762) received a 510(k) decision of Substantially Equivalent on August 2, 1984, 97 days after the submission was received.

What is the product code of K841762?

The FDA product code is HKX – Tonometer, Ac-Powered, a Class II (moderate risk) device regulated under 21 CFR 886.1930.