510(k) K062751
K062751 is an FDA 510(k) premarket notification submitted by Quantimetrix Corp. for the device "MODIFICATION TO QUANTIMETRIX CARDIASURE CARDIAC MARKER". The FDA issued a decision of Substantially Equivalent on October 3, 2006. The device falls under product code JJT (Enzyme Controls (Assayed And Unassayed)), a Class I device regulated under 21 CFR 862.1660. Quantimetrix Corp. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- October 3, 2006
- Date Received
- September 14, 2006
- Clearance Type
- Special
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Enzyme Controls (Assayed And Unassayed)
- Device Class
- Class I
- Regulation Number
- 862.1660
- Review Panel
- CH
- Submission Type