510(k) K082499

C. DIFF QUIK CHEK COMPLETE by Techlab, Inc. — Product Code LLH

K082499 is an FDA 510(k) premarket notification submitted by Techlab, Inc. for the device "C. DIFF QUIK CHEK COMPLETE". The FDA issued a decision of Substantially Equivalent on March 26, 2009. The device falls under product code LLH (Reagents, Clostridium Difficile Toxin), a Class I device regulated under 21 CFR 866.2660. Techlab, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 26, 2009
Date Received
August 29, 2008
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Reagents, Clostridium Difficile Toxin
Device Class
Class I
Regulation Number
866.2660
Review Panel
MI
Submission Type