Home / 510(k) Clearances / K921024

510(k) K921024

URO-TOTE LEG BAG by Neotech Products, Inc. — Product Code KNX

K921024 is an FDA 510(k) premarket notification submitted by Neotech Products, Inc. for the device "URO-TOTE LEG BAG". The FDA issued a decision of Substantially Equivalent on September 2, 1992. The device falls under product code KNX (Collector, Urine, (And Accessories) For Indwelling Catheter), a Class II device regulated under 21 CFR 876.5250. Neotech Products, Inc. has at least 5 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 2, 1992
Date Received
March 3, 1992
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Collector, Urine, (And Accessories) For Indwelling Catheter
Device Class
Class II
Regulation Number
876.5250
Review Panel
GU
Submission Type

Other clearances by Neotech Products, Inc.

  • K011564 — NEOLEAD (January 3, 2002)
  • K931727 — URINARY DRAINAGE BAG CADDY (July 23, 1993)
  • K890425 — NEOTECH MUCUS TRAP W/CATHETER (April 19, 1989)
  • K882203 — NEOTECH UNIVERSAL ADAPTER (June 17, 1988)
  • K880487 — NEOTECH MECONIUM ASPIRATOR (STERILE) (May 6, 1988)

Other clearances for product code KNX

  • K110518 — IBAG (June 24, 2011)
  • K973364 — 4L DRAINAGE BAG, 4L BAG FOR PERITONEAL DIALYSIS, 4L URINARY DRAINAGE BAG (March 17, 1998)
  • K972887 — MEDLINE PREMIUM LEG BAG, MEDLINE FABRIC BAC LEG BAG, MEDLINE URINARY LEG BAG (December 11, 1997)
  • K971271 — BESECURE EXTERNAL URINARY COLLECTION SYSTEM (August 18, 1997)
  • K971929 — AMSINO URINARY LEG BAG (August 6, 1997)
  • K971764 — WELCON HUE-VU URINARY DRAINAGE BAG (July 29, 1997)
  • K964690 — LIBERTY VALVE (March 21, 1997)
  • K964745 — AMSINO URINARY DRAINAGE BAG (March 18, 1997)
  • K962652 — URINARY DRAINAGE BAG, (REORDER NO. 0749 - PRODUCT NO. 900-749) (October 4, 1996)
  • K960949 — PROSYS BEDSIDE DRAINAGE BAG (STERILE) MODEL 650167 (April 19, 1996)

FDA data resources