510(k) K931336

DRS 4 DIALYZER REPROCESSING SYSTEM by Seratronics, Inc. — Product Code LIF

K931336 is an FDA 510(k) premarket notification submitted by Seratronics, Inc. for the device "DRS 4 DIALYZER REPROCESSING SYSTEM". The FDA issued a decision of Substantially Equivalent on April 18, 1996. The device falls under product code LIF (Dialyzer Reprocessing System), a Class II device regulated under 21 CFR 876.5820. Seratronics, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 18, 1996
Date Received
March 16, 1993
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