THE FUGO BLADE— 510(k) K001498

Substantially Equivalent

Medisurg , Ltd.

FDA 510(k) clearance K001498 for THE FUGO BLADE, Substantially Equivalent on 2000-08-10. 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: 2000-05-15
Decision date: 2000-08-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Norristown, PA, US

Download summary PDF View on FDA.gov ↗

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