510(k) K833181

HPR HOME PATIENT RENATRON by Renal Systems, Inc. — Product Code LIF

K833181 is an FDA 510(k) premarket notification submitted by Renal Systems, Inc. for the device "HPR HOME PATIENT RENATRON". The FDA issued a decision of Substantially Equivalent on October 27, 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
October 27, 1983
Date Received
September 19, 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