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

(STAMEY) T.U.R.P. SUPRAPUBIC CATHETER SET

K Number: K863120 · Decision Oct 24, 1986
Classifications
1
FEI Numbers
24
Registration Numbers
24
Same Product Code
31
Applicant Total
104
Review Days
71

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Basic Information

Device Name
(STAMEY) T.U.R.P. SUPRAPUBIC CATHETER SET
K Number
K863120
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5090
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
Cook Urological, Inc.
Date Received
August 14, 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)

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