FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

MUTO BRUSH

K Number: K833330 · Decision Nov 14, 1983
Classifications
1
FEI Numbers
44
Registration Numbers
44
Same Product Code
43
Applicant Total
18
Review Days
48

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Basic Information

Device Name
MUTO BRUSH
K Number
K833330
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1500
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
Microvasive
Date Received
September 27, 1983
Decision Date
November 14, 1983
Product Code
FDX
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
FDX Endoscopic Cytology Brush

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Other Clearances by Microvasive

K Number Device Name
K872771 LOW PROFILE GASTROSTOMY
K870705 THERMAL COAGULATOR
K861309 JEJUNAL FEEDING TUBE
K861323 REPLACEMENT GASTROSTOMY TUBE
K860589 INFLATOR/DEFLATOR PISTON SYRINGE
K860366 CHALLENGER HOT BIOPSY FORCEPS
K854238 NEEDLE W/STYLET FOR IMPLANTATION
K854063 MICROVASIVE SILICONE SPRAY
K851652 PAPILLOTOME
K850393 FLEXIBLE FIBEROPTIC ENDOSCOPE
Search all 18 clearances from Microvasive →