The following data is part of a premarket notification filed by Exigent Diagnostics, Inc. with the FDA for Careside Total Protein.
Device ID | K980042 |
510k Number | K980042 |
Device Name: | CARESIDE TOTAL PROTEIN |
Classification | Biuret (colorimetric), Total Protein |
Applicant | EXIGENT DIAGNOSTICS, INC. 6100 BRISTOL PKWY. Culver City, CA 90230 |
Contact | Kenneth B Asarch |
Correspondent | Kenneth B Asarch EXIGENT DIAGNOSTICS, INC. 6100 BRISTOL PKWY. Culver City, CA 90230 |
Product Code | CEK |
CFR Regulation Number | 862.1635 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1998-01-06 |
Decision Date | 1998-02-04 |
Summary: | summary |