510(k) K010855

RANDOX IGE by Randox Laboratories, Ltd. — Product Code DGC

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 15, 2001
Date Received
March 22, 2001
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

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