510(k) K831987

EPSILON IGE TEST KIT by Beckman Instruments, Inc. — Product Code DGO

K831987 is an FDA 510(k) premarket notification submitted by Beckman Instruments, Inc. for the device "EPSILON IGE TEST KIT". The FDA issued a decision of Substantially Equivalent on October 14, 1983. The device falls under product code DGO (Ige, Peroxidase, 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
October 14, 1983
Date Received
June 21, 1983
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Ige, Peroxidase, Antigen, Antiserum, Control
Device Class
Class II
Regulation Number
866.5510
Review Panel
PA
Submission Type