The following data is part of a premarket notification filed by Clinical Data, Inc. with the FDA for In-vitro Test For The Determination Of Cholesterol.
Device ID | K854179 |
510k Number | K854179 |
Device Name: | IN-VITRO TEST FOR THE DETERMINATION OF CHOLESTEROL |
Classification | Enzymatic Esterase--oxidase, Cholesterol |
Applicant | CLINICAL DATA, INC. 1172 COMMONWEALTH AVE. Boston, MA 02134 |
Contact | Israel M Stein |
Correspondent | Israel M Stein CLINICAL DATA, INC. 1172 COMMONWEALTH AVE. Boston, MA 02134 |
Product Code | CHH |
CFR Regulation Number | 862.1175 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1985-10-15 |
Decision Date | 1985-11-25 |