510(k) K902202

DMA TRIGLYCERIDE (GPO) PROCEDURE by Data Medical Associates, Inc. — Product Code JGY

K902202 is an FDA 510(k) premarket notification submitted by Data Medical Associates, Inc. for the device "DMA TRIGLYCERIDE (GPO) PROCEDURE". The FDA issued a decision of Substantially Equivalent on July 31, 1990. The device falls under product code JGY (Colorimetric Method, 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
July 31, 1990
Date Received
May 16, 1990
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Colorimetric Method, Triglycerides
Device Class
Class I
Regulation Number
862.1705
Review Panel
CH
Submission Type