510(k) K864312

IC MICROASSAY by Diamedix Corp. — Product Code DAK

K864312 is an FDA 510(k) premarket notification submitted by Diamedix Corp. for the device "IC MICROASSAY". The FDA issued a decision of Substantially Equivalent on January 9, 1987. The device falls under product code DAK (Complement C1q, Antigen, Antiserum, Control), a Class II device regulated under 21 CFR 866.5240. Diamedix Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 9, 1987
Date Received
November 3, 1986
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Complement C1q, Antigen, Antiserum, Control
Device Class
Class II
Regulation Number
866.5240
Review Panel
IM
Submission Type