510(k) K965213

STRATUS MYOGLOBIN GLUOROMETRIC ENZYME IMMUNOASSAY by Dade Intl., Inc. — Product Code DDR

K965213 is an FDA 510(k) premarket notification submitted by Dade Intl., Inc. for the device "STRATUS MYOGLOBIN GLUOROMETRIC ENZYME IMMUNOASSAY". The FDA issued a decision of Substantially Equivalent on February 10, 1997. The device falls under product code DDR (Myoglobin, Antigen, Antiserum, Control), a Class II device regulated under 21 CFR 866.5680. Dade Intl., Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 10, 1997
Date Received
December 30, 1996
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