510(k) K944539

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

K944539 is an FDA 510(k) premarket notification submitted by Seratronics, Inc. for the device "DRS 4 ND DIALYZER REPROCESSING SYSTEM". The FDA issued a decision of Substantially Equivalent on November 29, 1995. 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
November 29, 1995
Date Received
September 15, 1994
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