510(k) K073487

OLYMPUS IGM REAGENT by Olympus America, Inc. — Product Code CFN

K073487 is an FDA 510(k) premarket notification submitted by Olympus America, Inc. for the device "OLYMPUS IGM REAGENT". The FDA issued a decision of Substantially Equivalent on February 11, 2008. The device falls under product code CFN (Method, Nephelometric, Immunoglobulins (G, A, M)), a Class II device regulated under 21 CFR 866.5510. Olympus America, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 11, 2008
Date Received
December 12, 2007
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Method, Nephelometric, Immunoglobulins (G, A, M)
Device Class
Class II
Regulation Number
866.5510
Review Panel
IM
Submission Type