Phase II Digoxin Radioimmunoassay Kit
FDA 510(k) K830533 · Medical & Scientific Designs, Inc.
510(k) numberK830533
Submission
- Device name
- Phase II Digoxin Radioimmunoassay Kit
- Applicant
- Medical & Scientific Designs, Inc.
Mchenry, IL, US - Received
- February 18, 1983
- Decision date
- April 5, 1983
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
- Product code
- DON – Radioimmunoassay, Digoxin (125-I), Rabbit Antibody, Solid Phase Sep.
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 862.3320
- Specialty
- Clinical Toxicology
Other 510(k)s with product code DON
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K902861 | Ciba Corning Acs Digoxin ImmunoassayDON · Traditional | Ciba Corning Diagnostics Corp. | 09/10/1990SE |
| K881679 | Ciba Corning Magic Lite Digoxin ImmunoassayDON · Traditional | Ciba Corning Diagnostics Corp. | 07/08/1988SE |
| K840461 | Magic 125I Digoxin RadioimmunoassayDON · Traditional | Corning Medical & Scientific | 03/23/1984SE |
| K822053 | Zetaphase-DigDON · Traditional | Biological & Diagnostic Products | 07/27/1982SE |
| K821000 | Enzymune-Test DigoxinDON · Traditional | Icl Scientific | 04/26/1982SE |
| K810296 | Digoxin Ria AssayDON · Traditional | Ria Diagnostics | 02/19/1981SE |
| K803075 | Digoxin Riabead Diagnostic KitDON · Traditional | Abbott Laboratories | 12/22/1980SE |
| K791549 | Technicon Star SystemDON · Traditional | Technicon Instruments Corp. | 09/27/1979SE |
| K781660 | Ria, DigoxinDON · Traditional | E. R. Squibb & Sons, Inc. | 10/24/1978SE |
| K780475 | Dac-Cel Digoxin Radioimmunoassay KitDON · Traditional | Burroughs Wellcome Co. | 04/24/1978SE |
More from Burroughs Wellcome Co.
| 510(k) | Device | Decision |
|---|---|---|
| K862960 | Phase II Ferritin Radioimmunoassay KitDBF · Traditional | 08/27/1986SE |
| K853224 | Phase II B-12/FOLATE KitCDD · Traditional | 10/03/1985SE |
| K840901 | Phase II Free T4 KitCEC · Traditional | 04/25/1984SE |
| K840328 | Phase II HCG KitJHI · Traditional | 04/19/1984SE |
| K834219 | Phase II Cortisol KitCGR · Traditional | 02/04/1984SE |
| K833789 | Phase II Theophylline RadioimmunoassayLCA · Traditional | 01/24/1984SE |
| K832499 | Phase II TSH KitJLW · Traditional | 09/12/1983SE |
| K832210 | Gamma Photon Gamma CounterJJJ · Traditional | 08/24/1983SE |
| K832209 | Kineti Count 24 Gamma CounterJJJ · Traditional | 08/24/1983SE |
| K831064 | Phase II T3 Radioimmunoassay KitCDP · Traditional | 05/09/1983SE |
Questions and answers
When was Phase II Digoxin Radioimmunoassay Kit cleared by the FDA?
Phase II Digoxin Radioimmunoassay Kit (K830533) received a 510(k) decision of Substantially Equivalent on April 5, 1983, 46 days after the submission was received.
What is the product code of K830533?
The FDA product code is DON – Radioimmunoassay, Digoxin (125-I), Rabbit Antibody, Solid Phase Sep., a Class II (moderate risk) device regulated under 21 CFR 862.3320.