MUTO BRUSH— 510(k) K833330

Substantially Equivalent

Microvasive

FDA 510(k) clearance K833330 for MUTO BRUSH, Substantially Equivalent on 1983-11-14. Applicant: Microvasive. Device class: 2.

Clearance details

Applicant: Microvasive
Product code: Code FDX
Device class: Class 2
Regulation: 21 CFR 876.1500
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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More clearances from Microvasive

K872771 — LOW PROFILE GASTROSTOMY1987-10-09
K870705 — THERMAL COAGULATOR1987-04-17
K861309 — JEJUNAL FEEDING TUBE1986-12-16
K861323 — REPLACEMENT GASTROSTOMY TUBE1986-12-16
K860366 — CHALLENGER HOT BIOPSY FORCEPS1986-04-07

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