The following data is part of a premarket notification filed by Bioclinical Systems, Inc. with the FDA for Bcs Potassium Turbidimetric Test.
| Device ID | K850258 |
| 510k Number | K850258 |
| Device Name: | BCS POTASSIUM TURBIDIMETRIC TEST |
| Classification | Tetraphenyl Borate, Colorimetry, Potassium |
| Applicant | BIOCLINICAL SYSTEMS, INC. 5977 SOUTHWEST AVE. St.louis, MO 63139 |
| Contact | Bruce F Watkins |
| Correspondent | Bruce F Watkins BIOCLINICAL SYSTEMS, INC. 5977 SOUTHWEST AVE. St.louis, MO 63139 |
| Product Code | CEJ |
| CFR Regulation Number | 862.1600 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1985-01-22 |
| Decision Date | 1985-02-07 |