KEELER APPLANATION TONOMETER; T-TYPE KAT, K-TYPE KAT, (KAT)— 510(k) K093445

Name: FDA 510(k) clearance K093445
Creator: U.S. Food and Drug Administration
Published: 2010-01-19

Substantially Equivalent

Keeler, Ltd.

FDA 510(k) clearance K093445 for KEELER APPLANATION TONOMETER; T-TYPE KAT, K-TYPE KAT, (KAT), Substantially Equivalent on 2010-01-19. Applicant: Keeler, Ltd.. Device class: 2.

Clearance details

Applicant: Keeler, Ltd.
Product code: Code HKY
Device class: Class 2
Regulation: 21 CFR 886.1930
Advisory panel: Ophthalmic
Date received: 2009-10-21
Decision date: 2010-01-19
Decision: Substantially Equivalent
Clearance type: Abbreviated
Location: Broomall, PA, US

Download summary PDF View on FDA.gov ↗

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