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

VESICO SUPRAPUBIC BLADDER DRAINAGE & EXCHANGE SETS

K Number: K863386 · Decision Oct 24, 1986
Classifications
1
FEI Numbers
24
Registration Numbers
24
Same Product Code
31
Applicant Total
24
Review Days
51

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Basic Information

Device Name
VESICO SUPRAPUBIC BLADDER DRAINAGE & EXCHANGE SETS
K Number
K863386
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5090
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
Angiomed U.S., Inc.
Date Received
September 3, 1986
Decision Date
October 24, 1986
Product Code
KOB
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
KOB Catheter, Suprapubic (And Accessories)

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (KOB), ordered by most recent decision date.

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Other Clearances by Angiomed U.S., Inc.

K Number Device Name
K874771 ANGIOMED INTRODUCING SETS
K874585 ANGIOMED OSTY-CUT BONE BIOPSY NEEDLE
K864225 ANGIOMED URETERAL D&M SETS/URETEROSCOPY GUID STENT
K862805 ANGIOMED VAC-U-CUT BIOPSY NEEDLE
K863446 ANGIOMED HIGH PRESSURE CONNECTORS
K854910 ANGIOFLOW
K854912 ANGIOMED GUIED WIRES
K854908 UROFLEX
K855142 ANGIOMED PERCUTANEOUS TRANSHEPATIC CHOLANGIOGTAPHY
K855076 ANGIOMED URETER DIATION SETS
Search all 24 clearances from Angiomed U.S., Inc. →