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

APEX(TM) PROSTATIC BALLOON DILATION CATHETER

K Number: K913477 · Decision Dec 27, 1991
Classifications
1
FEI Numbers
68
Registration Numbers
68
Same Product Code
26
Applicant Total
17
Review Days
144

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Basic Information

Device Name
APEX(TM) PROSTATIC BALLOON DILATION CATHETER
K Number
K913477
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5520
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Peripheral Systems Group
Date Received
August 5, 1991
Decision Date
December 27, 1991
Product Code
KOE
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
KOE Dilator, Urethral

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K915168 PROFLEX 5
K913746 SMARTNEEDLE(TM) VASCULAR ACCESS SYSTEM
K904984 ADVANCE 418(TM)
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