Medical & Scientific Designs, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 14
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K862960 | PHASE II FERRITIN RADIOIMMUNOASSAY KIT | August 27, 1986 |
| K853224 | PHASE II B-12/FOLATE KIT | October 3, 1985 |
| K840901 | PHASE II FREE T4 KIT | April 25, 1984 |
| K840328 | PHASE II HCG KIT | April 19, 1984 |
| K834219 | PHASE II CORTISOL KIT | February 4, 1984 |
| K833789 | PHASE II THEOPHYLLINE RADIOIMMUNOASSAY | January 24, 1984 |
| K832499 | PHASE II TSH KIT | September 12, 1983 |
| K832210 | GAMMA PHOTON GAMMA COUNTER | August 24, 1983 |
| K832209 | KINETI COUNT 24 GAMMA COUNTER | August 24, 1983 |
| K831064 | PHASE II T3 RADIOIMMUNOASSAY KIT | May 9, 1983 |
| K830900 | UPTAKE T3 RADIOIMMUNOASSAY KIT | April 18, 1983 |
| K830533 | PHASE II DIGOXIN RADIOIMMUNOASSAY KIT | April 5, 1983 |
| K830642 | PHASE THYROXINE RADIOIMMUNOASSAY KIT | April 5, 1983 |
| K830365 | KINETI COUNT 48 IMMUNOASSAY SYSTEM | March 10, 1983 |