510(k) K042924

ARCHITECT STAT MYO IMMUNOASSAY by Fisher Diagnostics — Product Code DDR

K042924 is an FDA 510(k) premarket notification submitted by Fisher Diagnostics for the device "ARCHITECT STAT MYO IMMUNOASSAY". The FDA issued a decision of Substantially Equivalent on January 24, 2005. The device falls under product code DDR (Myoglobin, Antigen, Antiserum, Control), a Class II device regulated under 21 CFR 866.5680. Fisher Diagnostics has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 24, 2005
Date Received
October 22, 2004
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Myoglobin, Antigen, Antiserum, Control
Device Class
Class II
Regulation Number
866.5680
Review Panel
IM
Submission Type