Keeler Tearscope-Plus

FDA 510(k) K973064 · Keeler Instruments, Inc.

Substantially Equivalent

510(k) numberK973064

Submission

Device name
Keeler Tearscope-Plus
Applicant
Keeler Instruments, Inc.
Broomall, PA, US
Received
August 18, 1997
Decision date
April 7, 1998
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
HJO – Biomicroscope, Slit-Lamp, Ac-Powered
Device class
Class II (moderate risk)
Regulation
21 CFR 886.1850
Specialty
Ophthalmic

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Questions and answers

When was Keeler Tearscope-Plus cleared by the FDA?

Keeler Tearscope-Plus (K973064) received a 510(k) decision of Substantially Equivalent on April 7, 1998, 232 days after the submission was received.

What is the product code of K973064?

The FDA product code is HJO – Biomicroscope, Slit-Lamp, Ac-Powered, a Class II (moderate risk) device regulated under 21 CFR 886.1850.