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

SEXTON CYSTOTOMY URINE PUMP (SCUP2)

K Number: K904434 · Decision Feb 1, 1991
Classifications
1
FEI Numbers
24
Registration Numbers
24
Same Product Code
31
Applicant Total
3
Review Days
126

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Basic Information

Device Name
SEXTON CYSTOTOMY URINE PUMP (SCUP2)
K Number
K904434
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5090
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
Phoenix Bioengineering, Inc.
Date Received
September 28, 1990
Decision Date
February 1, 1991
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 Phoenix Bioengineering, Inc.

K Number Device Name
K930125 PHOENIX BONE SCREWS PBS-TYPE SERIES
K913490 PHOENIX BURR HOLE BUTTON, BURR 1