510(k) K884353
K884353 is an FDA 510(k) premarket notification submitted by Cd Medical, Inc. for the device "ULTRX(TM) 850 ARTIFICIAL KIDNEY". The FDA issued a decision of Substantially Equivalent on December 8, 1988. The device falls under product code KDI (Dialyzer, High Permeability With Or Without Sealed Dialysate System), a Class II device regulated under 21 CFR 876.5860. Cd Medical, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- December 8, 1988
- Date Received
- October 17, 1988
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Dialyzer, High Permeability With Or Without Sealed Dialysate System
- Device Class
- Class II
- Regulation Number
- 876.5860
- Review Panel
- GU
- Submission Type