The following data is part of a premarket notification filed by Cholestech Corp. with the FDA for Cholestech Lipid Monitor Syst, Triglycerides Test.
Device ID | K914033 |
510k Number | K914033 |
Device Name: | CHOLESTECH LIPID MONITOR SYST, TRIGLYCERIDES TEST |
Classification | Colorimetric Method, Triglycerides |
Applicant | CHOLESTECH CORP. 3347 INVESTMENT BLVD. Hayward, CA 94545 |
Contact | Susan Willson |
Correspondent | Susan Willson CHOLESTECH CORP. 3347 INVESTMENT BLVD. Hayward, CA 94545 |
Product Code | JGY |
CFR Regulation Number | 862.1705 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1991-09-10 |
Decision Date | 1991-09-27 |