MUTO BRUSH— 510(k) K833330

Substantially Equivalent

Microvasive

FDA 510(k) clearance K833330 for MUTO BRUSH, Substantially Equivalent on 1983-11-14. Applicant: Microvasive.

Clearance details

Applicant: Microvasive
Product code: Code FDX
Advisory panel: Gastroenterology, Urology
Date received: 1983-09-27
Decision date: 1983-11-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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