510(k) K050891

TOX A/B QUICK CHEK by Techlab, Inc. — Product Code LLH

K050891 is an FDA 510(k) premarket notification submitted by Techlab, Inc. for the device "TOX A/B QUICK CHEK". The FDA issued a decision of Substantially Equivalent on July 25, 2005. 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
July 25, 2005
Date Received
April 8, 2005
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