510(k) K022550

COAMATIC LR ANTITHROMBIN, NOTE: LR=LIQUID REAGENTS by Instrumentation Laboratory CO — Product Code JBQ

K022550 is an FDA 510(k) premarket notification submitted by Instrumentation Laboratory CO for the device "COAMATIC LR ANTITHROMBIN, NOTE: LR=LIQUID REAGENTS". The FDA issued a decision of Substantially Equivalent on August 27, 2002. The device falls under product code JBQ (Antithrombin Iii Quantitation), a Class II device regulated under 21 CFR 864.7060. Instrumentation Laboratory CO has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 27, 2002
Date Received
August 2, 2002
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Antithrombin Iii Quantitation
Device Class
Class II
Regulation Number
864.7060
Review Panel
HE
Submission Type