510(k) K830574
K830574 is an FDA 510(k) premarket notification submitted by Renal Systems, Inc. for the device "RENATRON DIALYZER REPROCESSING SYS". The FDA issued a decision of Substantially Equivalent on March 29, 1983. The device falls under product code LIF (Dialyzer Reprocessing System), a Class II device regulated under 21 CFR 876.5820. Renal Systems, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- March 29, 1983
- Date Received
- February 23, 1983
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Dialyzer Reprocessing System
- Device Class
- Class II
- Regulation Number
- 876.5820
- Review Panel
- GU
- Submission Type