510(k) K991796

IMMULITE TURBO MYOGLOBIN, MODELS LSKMY1, LSKMY5 by Diagnostic Products Corp. — Product Code DDR

K991796 is an FDA 510(k) premarket notification submitted by Diagnostic Products Corp. for the device "IMMULITE TURBO MYOGLOBIN, MODELS LSKMY1, LSKMY5". The FDA issued a decision of Substantially Equivalent on June 9, 1999. 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
June 9, 1999
Date Received
May 26, 1999
Clearance Type
Special
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