510(k) K030404
K030404 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 April 24, 2003. 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
- April 24, 2003
- Date Received
- February 6, 2003
- 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