510(k) K960474
K960474 is an FDA 510(k) premarket notification submitted by Cobe Renal Care, Inc. for the device "COBE CENTRYSYSTEM 600 HG HEMODIALYZERS". The FDA issued a decision of Substantially Equivalent on August 14, 1996. 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. Cobe Renal Care, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- August 14, 1996
- Date Received
- February 2, 1996
- 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