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

NOPROFILE OLBERT CATHETER SYSTEM

K Number: K945061 · Decision Mar 9, 1995
Classifications
1
FEI Numbers
114
Registration Numbers
114
Same Product Code
237
Applicant Total
24
Review Days
146

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Basic Information

Device Name
NOPROFILE OLBERT CATHETER SYSTEM
K Number
K945061
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5130
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Meadox Surgimed, Inc.
Date Received
October 14, 1994
Decision Date
March 9, 1995
Product Code
KOD
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
KOD Catheter, Urological

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K911635 MEADOX(R) SURGIMED(R) BIOPSY GUN II
K905181 NO PROFILE OLBERT CATHETER SYSTEM FOR UROLOGY
K904582 QUICKWIRE - HYDROPHILIC COATED GUIDEWIRE
K904983 MEADOX(R) SURGIMED OLBERT CATH SYST FOR UROLOGY
K902461 MEADOX SURGIMED BIOPSY GUN AND NEEDLE
K890926 SURECUT BMB BONE MARROW BIOPSY/ASPIRATION NEEDLE
K863218 CYTOSTATIC FILTRATION SET
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