PROSYS BEDSIDE DRAINAGE BAG (STERILE) MODEL 650167— 510(k) K960949

Name: FDA 510(k) clearance K960949
Creator: U.S. Food and Drug Administration
Published: 1996-04-19

Substantially Equivalent

Bristol-Myers Squibb

FDA 510(k) clearance K960949 for PROSYS BEDSIDE DRAINAGE BAG (STERILE) MODEL 650167, Substantially Equivalent on 1996-04-19. Applicant: Bristol-Myers Squibb. Device class: 2.

Clearance details

Applicant: Bristol-Myers Squibb
Product code: Code KNX
Device class: Class 2
Regulation: 21 CFR 876.5250
Advisory panel: Gastroenterology, Urology
Date received: 1996-03-11
Decision date: 1996-04-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Skillman, NJ, US

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K110518 — IBAG2011-06-24
K973364 — 4L DRAINAGE BAG, 4L BAG FOR PERITONEAL DIALYSIS, 4L URINARY DRAINAGE BAG1998-03-17
K972887 — MEDLINE PREMIUM LEG BAG, MEDLINE FABRIC BAC LEG BAG, MEDLINE URINARY LEG BAG1997-12-11
K971271 — BESECURE EXTERNAL URINARY COLLECTION SYSTEM1997-08-18
K971929 — AMSINO URINARY LEG BAG1997-08-06

Adverse events under product code KNX

product code KNX

Malfunction: 1,064
Total: 1,064

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.