PANORET, MODEL 1000A— 510(k) K001111

Name: FDA 510(k) clearance K001111
Creator: U.S. Food and Drug Administration
Published: 2000-07-07

Substantially Equivalent

Cmt Medical Technologies, Ltd.

FDA 510(k) clearance K001111 for PANORET, MODEL 1000A, Substantially Equivalent on 2000-07-07. Applicant: Cmt Medical Technologies, Ltd.. Device class: 2.

Clearance details

Applicant: Cmt Medical Technologies, Ltd.
Product code: Code HKL
Device class: Class 2
Regulation: 21 CFR 886.1780
Advisory panel: Ophthalmic
Date received: 2000-04-06
Decision date: 2000-07-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Haifa, IL

Download summary PDF View on FDA.gov ↗

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