Clinical Technology Corp.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 12
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K925080 | TEK-LUBE | January 31, 1994 |
| K872867 | BIOSIGN | July 6, 1988 |
| K880166 | BOVIE ULTRASONIC SURGICAL ASPIRATOR, MODEL ME2000 | February 18, 1988 |
| K872705 | BOVIE 400-CT ELECTROSURGICAL GENERATOR (UNIT) | September 1, 1987 |
| K855138 | BOVIE ULTRASONIC SURGICAL SYSTEM | November 10, 1986 |
| K854231 | ELECTROSURGICAL CUTTING & COAGULATION DEVICE/ACCES | May 2, 1986 |
| K853507 | STERI-GRIP | September 5, 1985 |
| K852986 | GLYCO-SEP/ALC TEST KIT FOR SEPARAT OF HEMOGLOBIN | August 19, 1985 |
| K844565 | BOVIE X-10 ELECTROSURGICAL GENERATOR(UNIT) | February 21, 1985 |
| K841272 | SICKLE-STAT HEMOGLOBIN S SCREEN KIT | April 13, 1984 |
| K823077 | URINARY BLADDER TEMP. SENSOR #81-003 | March 9, 1983 |
| K813000 | DISPOSABLE ARTHROSCOPY CANNULA SET | January 22, 1982 |