510(k) K965108

SYNCHRON LX SYSTEMS IMMUNOGLOBULIN G/A/M REAGENT by Beckman Instruments, Inc. — Product Code DEW

K965108 is an FDA 510(k) premarket notification submitted by Beckman Instruments, Inc. for the device "SYNCHRON LX SYSTEMS IMMUNOGLOBULIN G/A/M REAGENT". The FDA issued a decision of Substantially Equivalent on March 6, 1997. The device falls under product code DEW (Igg, Antigen, Antiserum, Control), a Class II device regulated under 21 CFR 866.5510. Beckman Instruments, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 6, 1997
Date Received
December 20, 1996
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Igg, Antigen, Antiserum, Control
Device Class
Class II
Regulation Number
866.5510
Review Panel
IM
Submission Type