Conphar-Schioetz Tonometer

FDA 510(k) K813619 · Conphar, Inc.

Substantially Equivalent

510(k) numberK813619

Submission

Device name
Conphar-Schioetz Tonometer
Applicant
Conphar, Inc.
Mchenry, IL, US
Received
December 29, 1981
Decision date
February 24, 1982
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
HKY – Tonometer, Manual
Device class
Class II (moderate risk)
Regulation
21 CFR 886.1930
Specialty
Ophthalmic

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Questions and answers

When was Conphar-Schioetz Tonometer cleared by the FDA?

Conphar-Schioetz Tonometer (K813619) received a 510(k) decision of Substantially Equivalent on February 24, 1982, 57 days after the submission was received.

What is the product code of K813619?

The FDA product code is HKY – Tonometer, Manual, a Class II (moderate risk) device regulated under 21 CFR 886.1930.