PERKINS HAND-HELD APPLANATION TONOMETER— 510(k) K961512

Name: FDA 510(k) clearance K961512
Creator: U.S. Food and Drug Administration
Published: 1996-07-18

Substantially Equivalent

Clement Clarke, Inc.

FDA 510(k) clearance K961512 for PERKINS HAND-HELD APPLANATION TONOMETER, Substantially Equivalent on 1996-07-18. Applicant: Clement Clarke, Inc.. Device class: 2.

Clearance details

Applicant: Clement Clarke, Inc.
Product code: Code HKY
Device class: Class 2
Regulation: 21 CFR 886.1930
Advisory panel: Ophthalmic
Date received: 1996-04-19
Decision date: 1996-07-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: England, GB

Download summary PDF View on FDA.gov ↗

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