510(k) K894783
K894783 is an FDA 510(k) premarket notification submitted by Baxter Healthcare Corp for the device "PERITONEAL DIAL. TITA. CATH ADAPTER & LOCKING CAP". The FDA issued a decision of Substantially Equivalent on Sep 7, 1989. The device falls under product code KDJ (Set, Administration, For Peritoneal Dialysis, Disposable), a Class II device regulated under 21 CFR 876.5630. Baxter Healthcare Corp has 507 other 510(k) clearances on record.
Clearance details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Sep 7, 1989
- Date Received
- Jul 27, 1989
- 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
- 510(k)