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

GENT-L-KARE STERILE URINARY DRAINAGE BAG CENTER

K Number: K881213 · Decision Jul 28, 1988
Classifications
1
FEI Numbers
127
Registration Numbers
127
Same Product Code
205
Applicant Total
13
Review Days
129

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Basic Information

Device Name
GENT-L-KARE STERILE URINARY DRAINAGE BAG CENTER
K Number
K881213
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5250
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
Geneva Laboratories, Inc.
Date Received
March 21, 1988
Decision Date
July 28, 1988
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

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Other Clearances by Geneva Laboratories, Inc.

K Number Device Name
K881217 GENT-L-KARE STERILE URINARY LEG BAG
K881218 GENT-L-KARE CLEANSING ENEMA SET
K881216 GENT-L-KARE VAGINAL IRRIGATION SET
K861308 ACCUPAC CUSTOM PACK KERLIX SQUARES
K861219 ACCUPAC CUSTOM SKIN SCRUB KIT
K853265 ACCUPAC CUSTOM OPERATING ROOM PROCEDURE-DK876543
K843206 COOK COUNTY HOSPITAL DRESSING CHANGE SET
K844255 GENT-L-KARE STERILE I.V. START KIT
K843090 UNIVERSITY OF CHICAGO VASCULAR ANGIOGRAM
K830725 GENT-L-SPEC DISPOS. VAGINAL SPECULUM
Search all 13 clearances from Geneva Laboratories, Inc. →