510(k) K991665
K991665 is an FDA 510(k) premarket notification submitted by A.P. Total Care, Inc. for the device "HDL CHOLESTEROL, PRODUCT NO'S 124-01, CH102-01". The FDA issued a decision of Substantially Equivalent on August 10, 1999. 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. A.P. Total Care, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- August 10, 1999
- Date Received
- May 14, 1999
- 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