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

WILTEK CYTOLOGY BRUSH

K Number: K894863 · Decision Dec 21, 1989
Classifications
1
FEI Numbers
44
Registration Numbers
44
Same Product Code
43
Applicant Total
21
Review Days
143

Basic Information

Device Name
WILTEK CYTOLOGY BRUSH
K Number
K894863
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1500
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
Wiltek Medical, Inc.
Date Received
July 31, 1989
Decision Date
December 21, 1989
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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K Number Device Name
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K930419 WILTEK BIOPSY FORCEPS
K914882 WILTEK BALLOON CHOLANGIOGRAPHY CATHETER
K914881 WILTEK LAPAROSCOPIC CHOLANGIOGRAPHY CATHETER
K914132 WILTEK ELECTROCAUTERY ACTIVE CORD
K914131 WILTEK ELECTROCAUTERY ADAPTOR
K912122 CHOLANGIOGRAPHY CATHETER
K912288 WILTEK STANDARD CHOLANGIOGRAPHY CATHETER
K910334 ELECTROCAUTERY PROBE
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