510(k) K871301
K871301 is an FDA 510(k) premarket notification submitted by American Monitor Corp. for the device "ENZYMATIC TRIGLYCERIDES GPO-TRINDER METHOD". The FDA issued a decision of Substantially Equivalent on April 22, 1987. The device falls under product code CDT (Lipase Hydrolysis/Glycerol Kinase Enzyme, Triglycerides), a Class I device regulated under 21 CFR 862.1705. American Monitor Corp. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- April 22, 1987
- Date Received
- April 1, 1987
- 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