The following data is part of a premarket notification filed by Cholestech Corp. with the FDA for Cholestech Lipid Monitoring System, Total Choleste.
Device ID | K922612 |
510k Number | K922612 |
Device Name: | CHOLESTECH LIPID MONITORING SYSTEM, TOTAL CHOLESTE |
Classification | Enzymatic Esterase--oxidase, Cholesterol |
Applicant | CHOLESTECH CORP. 3347 INVESTMENT BLVD. Hayward, CA 94545 |
Contact | Gary Hewett |
Correspondent | Gary Hewett CHOLESTECH CORP. 3347 INVESTMENT BLVD. Hayward, CA 94545 |
Product Code | CHH |
CFR Regulation Number | 862.1175 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1992-06-02 |
Decision Date | 1992-06-24 |