510(k) K962652
K962652 is an FDA 510(k) premarket notification submitted by Customed, Inc. for the device "URINARY DRAINAGE BAG, (REORDER NO. 0749 - PRODUCT NO. 900-749)". The FDA issued a decision of Substantially Equivalent on October 4, 1996. The device falls under product code KNX (Collector, Urine, (And Accessories) For Indwelling Catheter), a Class II device regulated under 21 CFR 876.5250. Customed, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- October 4, 1996
- Date Received
- July 8, 1996
- 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