510(k) K850258
- Device
- BCS POTASSIUM TURBIDIMETRIC TEST
- Applicant
- BIOCLINICAL SYSTEMS, INC.
- 510(k) number
- K850258
- Product code
- CEJ
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1985-02-07
- Date received
- 1985-01-22
- Regulation
- 862.1600
- Classification name
- Tetraphenyl Borate, Colorimetry, Potassium
- Medical specialty
- Clinical Chemistry
- Review panel
- Clinical Chemistry
- Device class
- 2
- Clearance type
- Traditional
- Third party reviewed
- No
Applicant Contact#
- Contact
- BRUCE F WATKINS
- Address
- 5977 Southwest Ave. St.Louis MO US 63139 63139
FDA Registration Numbers#
- 2939693
- 3013660430
- 3004493545
- 1832216
Source Documents#
510(k) summary PDF not indicated by FDA
Other 510(k) Records For Product Code CEJ #
| 510(k) | Device | Applicant | Decision date |
|---|---|---|---|
| K043267 | POTASSIUM TEST KIT AND ELECTROLYTE CAL 1 AND 2 | Randox Laboratories, Ltd. | 2005-02-10 |
| K943026 | POTASSIUM QVET | Prisma Systems | 1994-12-09 |
| K904033 | REFLOTRON POTASSIUM TEST TABS | Boehringer Mannheim Corp. | 1990-11-06 |
| K902574 | POTASSIUM REAGENT SET | Tech-Co, Inc. | 1990-07-10 |
| K883585 | TECHNICON ASSIST POTASSIUM | Technicon Instruments Corp. | 1988-11-29 |
| K883586 | TECHNICON RA-100 SYSTEM POTASSIUM | Technicon Instruments Corp. | 1988-11-29 |
| K881440 | IQ POTASSIUM | Bd Becton Dickinson Vacutainer Systems Preanalytic | 1988-05-27 |
| K880339 | EASY-TEST POTASSIUM K ITEM NUMBER 19XXX | Em Diagnostic Systems, Inc. | 1988-02-25 |
| K863486 | POTASSIUM TEST | Sclavo, Inc. | 1986-09-29 |
| K861713 | SERUM POTASSIUM REAGENT SET | Sterling Diagnostics, Inc. | 1986-05-23 |
| K853404 | QCA POTASSIUM TEST KIT | Bd Becton Dickinson Vacutainer Systems Preanalytic | 1985-08-23 |
| K832553 | POTASSIUM TEST KIT | Mallinckrodt Critical Care | 1983-09-20 |
| K813608 | POTASSIUM REAGENT SET | Diagnostic Specialties | 1982-01-22 |
| K812677 | UNITEST-POTASSIUM | Biodynamics Corp. | 1981-10-02 |
| K811661 | POTASSIUM TEST | King Diagnostics, Inc. | 1981-06-25 |
Legacy Summary#
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FDA Review#
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