510(k) K082499
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