510(k) K863730

MYOLEX by Orion Corp. — Product Code DDR

K863730 is an FDA 510(k) premarket notification submitted by Orion Corp. for the device "MYOLEX". The FDA issued a decision of Substantially Equivalent on October 15, 1986. The device falls under product code DDR (Myoglobin, Antigen, Antiserum, Control), a Class II device regulated under 21 CFR 866.5680. Orion Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 15, 1986
Date Received
September 23, 1986
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