Cambridge Medical Technology
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 14
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
| K890837 | RIA-GNOST INSULIN | April 26, 1989 |
| K890697 | RIA-GNOST FERRITIN | March 16, 1989 |
| K890836 | RIA-GNOST PROGESTERONE | March 16, 1989 |
| K873737 | NO SPIN(TM) T3 COATED TUBE RADIOIMMUNOASSAY | November 24, 1987 |
| K870573 | T4 NO SPIN(TM) COATED TUBE RADIOIMMUNOASSAY KIT | April 22, 1987 |
| K862871 | RADIOIMMUNOASSAY OF NO SPIN(TM) CORTISOL | August 19, 1986 |
| K860130 | TESTOSTERONE COATED TUBES RADIOIMMUNOASSAY KIT | February 19, 1986 |
| K855169 | T3 UPTAKE RADIOIMMUNOASSAY KIT | February 6, 1986 |
| K850254 | PARATHYROID HORMONE RADIOIMMUNOASSAY KIT | April 3, 1985 |
| K843635 | MATCHED COMPONENT SET FOR RADIOIMMUNO- | September 28, 1984 |
| K841042 | MATCHED COMPONENT SET RADIOIMMUNOASSAY | April 19, 1984 |
| K834080 | MATCHED COMPONENT SET FOR DIGITOXIN | February 4, 1984 |
| K830148 | CORTISOL KIT | February 9, 1983 |
| K821811 | 125I DIGOXIN RADIOIMMUNOASSAY KIT | July 2, 1982 |