Clinical Technology Corp.
Clinical Technology Corp. holds FDA 510(k) medical device clearances, first cleared 1982, most recent 1994.
Top product codes for Clinical Technology Corp.
Recent clearances by Clinical Technology Corp.
- K925080 — TEK-LUBE
- K872867 — BIOSIGN
- K880166 — BOVIE ULTRASONIC SURGICAL ASPIRATOR, MODEL ME2000
- K872705 — BOVIE 400-CT ELECTROSURGICAL GENERATOR (UNIT)
- K855138 — BOVIE ULTRASONIC SURGICAL SYSTEM
- K854231 — ELECTROSURGICAL CUTTING & COAGULATION DEVICE/ACCES
- K853507 — STERI-GRIP
- K852986 — GLYCO-SEP/ALC TEST KIT FOR SEPARAT OF HEMOGLOBIN
- K844565 — BOVIE X-10 ELECTROSURGICAL GENERATOR(UNIT)
- K841272 — SICKLE-STAT HEMOGLOBIN S SCREEN KIT
- K823077 — URINARY BLADDER TEMP. SENSOR #81-003
- K813000 — DISPOSABLE ARTHROSCOPY CANNULA SET
Data sourced from openFDA. This site is unofficial and independent of the FDA.