FUGO BLADE FOR PERIPHERAL IRIDOTOMY, MODEL M300— 510(k) K050933

Name: FDA 510(k) clearance K050933
Creator: U.S. Food and Drug Administration
Published: 2005-12-09

Substantially Equivalent

Medisurg , Ltd.

FDA 510(k) clearance K050933 for FUGO BLADE FOR PERIPHERAL IRIDOTOMY, MODEL M300, Substantially Equivalent on 2005-12-09. Applicant: Medisurg , Ltd.. Device class: 2.

Clearance details

Applicant: Medisurg , Ltd.
Product code: Code NCR
Device class: Class 2
Regulation: 21 CFR 886.4100
Advisory panel: Ophthalmic
Date received: 2005-04-14
Decision date: 2005-12-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Norristown, PA, US

Download summary PDF View on FDA.gov ↗

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