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

ABSORBENT, DISPOSABLE URINARY DRAINAGE BAG

K Number: K901320 · Decision Jan 25, 1991
Classifications
1
FEI Numbers
127
Registration Numbers
127
Same Product Code
205
Applicant Total
3
Review Days
310

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Basic Information

Device Name
ABSORBENT, DISPOSABLE URINARY DRAINAGE BAG
K Number
K901320
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5250
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
Ep Medical, Inc.
Date Received
March 21, 1990
Decision Date
January 25, 1991
Product Code
KNX
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
KNX Collector, Urine, (And Accessories) For Indwelling Catheter

Similar 510(k) Clearances

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

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Other Clearances by Ep Medical, Inc.

K Number Device Name
K935590 EP MEDICAL, INC. EP-3 CLINICAL STIMULATOR
K933069 MODEL EP-2 CLINICAL STIMULATOR