KEELER DISPOSABLE TONOMATE, KEELER DISPOSABLE TONOMATE, BOX OF 100— 510(k) K152644

Name: FDA 510(k) clearance K152644
Creator: U.S. Food and Drug Administration
Published: 2015-12-31

Substantially Equivalent

Keeler Limited

FDA 510(k) clearance K152644 for KEELER DISPOSABLE TONOMATE, KEELER DISPOSABLE TONOMATE, BOX OF 100, Substantially Equivalent on 2015-12-31. Applicant: Keeler Limited. Device class: 2.

Clearance details

Applicant: Keeler Limited
Product code: Code HKY
Device class: Class 2
Regulation: 21 CFR 886.1930
Advisory panel: Ophthalmic
Date received: 2015-09-16
Decision date: 2015-12-31
Decision: Substantially Equivalent
Clearance type: Special
Location: Windsor, GB

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.