510(k) K870145
K870145 is an FDA 510(k) premarket notification submitted by Travenol Laboratories, S.A. for the device "EXTERNAL Y VALVE 5C4198". The FDA issued a decision of Substantially Equivalent on March 10, 1987. The device falls under product code KDJ (Set, Administration, For Peritoneal Dialysis, Disposable), a Class II device regulated under 21 CFR 876.5630. Travenol Laboratories, S.A. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- March 10, 1987
- Date Received
- January 13, 1987
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Set, Administration, For Peritoneal Dialysis, Disposable
- Device Class
- Class II
- Regulation Number
- 876.5630
- Review Panel
- GU
- Submission Type