510(k) K010700

RANDOX MYOGLOBIN by Randox Laboratories, Ltd. — Product Code DDR

K010700 is an FDA 510(k) premarket notification submitted by Randox Laboratories, Ltd. for the device "RANDOX MYOGLOBIN". The FDA issued a decision of Substantially Equivalent on May 8, 2001. The device falls under product code DDR (Myoglobin, Antigen, Antiserum, Control), a Class II device regulated under 21 CFR 866.5680. Randox Laboratories, Ltd. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 8, 2001
Date Received
March 8, 2001
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