510(k) K962199

QUANTEX C3 by Instrumentation Laboratory CO — Product Code CZW

K962199 is an FDA 510(k) premarket notification submitted by Instrumentation Laboratory CO for the device "QUANTEX C3". The FDA issued a decision of Substantially Equivalent on September 25, 1996. The device falls under product code CZW (Complement C3, Antigen, Antiserum, Control), a Class II device regulated under 21 CFR 866.5240. Instrumentation Laboratory CO has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 25, 1996
Date Received
June 7, 1996
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Complement C3, Antigen, Antiserum, Control
Device Class
Class II
Regulation Number
866.5240
Review Panel
IM
Submission Type