510(k) K971113

DMA TRIGLYCERIDES PROCEDURES by Data Medical Associates, Inc. — Product Code CDT

K971113 is an FDA 510(k) premarket notification submitted by Data Medical Associates, Inc. for the device "DMA TRIGLYCERIDES PROCEDURES". The FDA issued a decision of Substantially Equivalent on May 29, 1997. The device falls under product code CDT (Lipase Hydrolysis/Glycerol Kinase Enzyme, Triglycerides), a Class I device regulated under 21 CFR 862.1705. Data Medical Associates, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 29, 1997
Date Received
March 27, 1997
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