510(k) K003306

C. DIFFICILE TOX A/B II by Techlab, Inc. — Product Code LLH

K003306 is an FDA 510(k) premarket notification submitted by Techlab, Inc. for the device "C. DIFFICILE TOX A/B II". The FDA issued a decision of Substantially Equivalent on November 22, 2000. 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
November 22, 2000
Date Received
October 20, 2000
Clearance Type
Special
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