510(k) K812838
K812838 is an FDA 510(k) premarket notification submitted by Anco Medical Reagents & Assoc. for the device "TRIGLYCERIDE REAGENT SET". The FDA issued a decision of Substantially Equivalent on December 3, 1981. The device falls under product code CDT (Lipase Hydrolysis/Glycerol Kinase Enzyme, Triglycerides), a Class I device regulated under 21 CFR 862.1705. Anco Medical Reagents & Assoc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- December 3, 1981
- Date Received
- October 9, 1981
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Lipase Hydrolysis/Glycerol Kinase Enzyme, Triglycerides
- Device Class
- Class I
- Regulation Number
- 862.1705
- Review Panel
- CH
- Submission Type