Atlas FDA

URI-DRAIN COMBO KIT FOR MALE INCONTINENC

FDA 510(k) clearance K770789 · decided 1977-10-18

Clearance details

K-number
K770789
Device name
URI-DRAIN COMBO KIT FOR MALE INCONTINENC
Applicant
Chesebrough-Pond'S U.S.A. Co.
Decision
Substantially Equivalent
Date received
1977-05-03
Decision date
1977-10-18
Days to decision
168 days
Clearance type
Traditional
Product code
KNX
Device class
2
Regulation number
876.5250
Medical specialty
Gastroenterology, Urology
Advisory committee
Gastroenterology, Urology
Location
Mchenry, IL, 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
IBAG (K110518)Future Path Medical, LLC2011-06-24
4L DRAINAGE BAG, 4L BAG FOR PERITONEAL DIALYSIS, 4L URINARY DRAINAGE BAG (K973364)Maersk Medical A/S1998-03-17
MEDLINE PREMIUM LEG BAG, MEDLINE FABRIC BAC LEG BAG, MEDLINE URINARY LEG BAG (K972887)Medline Industries, Inc.1997-12-11
BESECURE EXTERNAL URINARY COLLECTION SYSTEM (K971271)Urology Research Intl., Inc.1997-08-18
AMSINO URINARY LEG BAG (K971929)Amsino Intl., Inc.1997-08-06
WELCON HUE-VU URINARY DRAINAGE BAG (K971764)Welcon, Inc.1997-07-29
LIBERTY VALVE (K964690)Cleveland Medical Devices, Inc.1997-03-21
AMSINO URINARY DRAINAGE BAG (K964745)Amsino Intl., Inc.1997-03-18
URINARY DRAINAGE BAG, (REORDER NO. 0749 - PRODUCT NO. 900-749) (K962652)Customed, Inc.1996-10-04
PROSYS BEDSIDE DRAINAGE BAG (STERILE) MODEL 650167 (K960949)Bristol-Myers Squibb1996-04-19
PROSYS LEG BAG (K952208)Convatec, A Division of E.R. Squibb & Sons1995-08-15
ORION'S URINARY DRAINAGE SET (K944377)Regulatory & Marketing Services, Inc.1994-12-06

Recalls involving this device

RecordFirmDate
URI-DRAIN Medium Male External Catheter With Two-Sided Adhesive Strap and Skin Protective recall (Z-2392-2011)Covidien LP2011-05-27
URI-DRAIN Standard Male External Catheter with Two-Sided Adhesive Strap and Skin Protectiv recall (Z-2393-2011)Covidien LP2011-05-27
URI-DRAIN Male Urinary Control Device - Large Product ID: 8884732598 (sold in Canada only) recall (Z-2394-2011)Covidien LP2011-05-27