Atlas FDA

FEMALE EXTERNAL URINARY COLLECTION POUCH

FDA 510(k) clearance K971499 · decided 1997-08-28

Clearance details

K-number
K971499
Device name
FEMALE EXTERNAL URINARY COLLECTION POUCH
Applicant
Mediquest, Inc.
Decision
Substantially Equivalent
Date received
1997-04-25
Decision date
1997-08-28
Days to decision
125 days
Clearance type
Traditional
Product code
EXI
Device class
1
Regulation number
876.5250
Medical specialty
Gastroenterology, Urology
Advisory committee
Gastroenterology, Urology
Location
Irvine, CA, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
HOLLISTER RETRACTED PENIS POUCH (K970443)Hollister, Inc.1997-02-25
BIODERM EID MALE EXTERNAL INCONTINENCE DEVICE (K963950)Bioderm, Inc.1997-01-10
HOLLISTER PREMIUM URINE COLLECTOR (K931277)Hollister, Inc.1993-06-23
CONVATEC LITTLE ONES PEDIATRIC URINE COLLECTION (K924755)Convatec, A Division of E.R. Squibb & Sons1993-06-22
CONVEEN(R) URISHEATH AND URILINER(MALE EXTER CATH) (K915246)Coloplast A/S1992-02-05
URIHESIVE STRIP (K915616)Convatec, A Division of E.R. Squibb & Sons1992-01-23

Recalls involving this device

No recalls on record reference this clearance.