510(k) K080125
K080125 is an FDA 510(k) premarket notification submitted by Wako Chemicals USA, Inc. for the device "APOLOWAKO T-CHO, HDL-C, TG AND ANALYZER, MODELS 993-23501, 999-23601, 995-23701 AND 993-25201". The FDA issued a decision of Substantially Equivalent on July 18, 2008. 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. Wako Chemicals USA, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- July 18, 2008
- Date Received
- January 17, 2008
- 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