510(k) K071706
K071706 is an FDA 510(k) premarket notification submitted by Clinical Data, Inc. for the device "ENVOY 500 HDL; CHOLESTEROL REAGENT KIT (MODEL# 55301), CALIBRATOR KIT (MODEL# 55118)". The FDA issued a decision of Substantially Equivalent on December 20, 2007. The device falls under product code LBS (Ldl & Vldl Precipitation, Cholesterol Via Esterase-Oxidase, Hdl), a Class I device regulated under 21 CFR 862.1475. Clinical Data, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- December 20, 2007
- Date Received
- June 21, 2007
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Ldl & Vldl Precipitation, Cholesterol Via Esterase-Oxidase, Hdl
- Device Class
- Class I
- Regulation Number
- 862.1475
- Review Panel
- CH
- Submission Type