FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

WURTZ CHOLEY CLIP (TM)

K Number: K901520 · Decision Jun 26, 1990
Classifications
1
FEI Numbers
57
Registration Numbers
57
Same Product Code
23
Applicant Total
11
Review Days
85

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Basic Information

Device Name
WURTZ CHOLEY CLIP (TM)
K Number
K901520
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4200
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Cd Medical, Inc.
Date Received
April 2, 1990
Decision Date
June 26, 1990
Product Code
GBZ
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

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

Product Code Device Name
GBZ Catheter, Cholangiography

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K884353 ULTRX(TM) 850 ARTIFICIAL KIDNEY
K880459 480 HIGH-FLOW ULTRAFILTRATION CONTROL DIALYSATE
K873279 8810 PUMP-PUMP SINGLE NEEDLE DEVICE
K864784 SERAFLO(TM) BLOODLINES FOR HEMODIALYSIS
K862304 DRAKE WILLOCK CENTRAL DIALYSATE DELIVERY SYSTEM
K853513 DRAKE WILLOCK 480 UF CONTROL IDALYSATE DELIVERY SY
K844185 MODIFIED C-DAK
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