510(k) K983970

IMMULITE MYOGLOBIN, MODEL LKMY1 AND LKMY5 by Diagnostic Products Corp. — Product Code DDR

K983970 is an FDA 510(k) premarket notification submitted by Diagnostic Products Corp. for the device "IMMULITE MYOGLOBIN, MODEL LKMY1 AND LKMY5". The FDA issued a decision of Substantially Equivalent on November 25, 1998. The device falls under product code DDR (Myoglobin, Antigen, Antiserum, Control), a Class II device regulated under 21 CFR 866.5680. Diagnostic Products Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 25, 1998
Date Received
November 9, 1998
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