Cavitron Corp.
Cavitron Corp. holds FDA 510(k) medical device clearances, first cleared 1976, most recent 1981.
Top product codes for Cavitron Corp.
Recent clearances by Cavitron Corp.
- K811582 — THE PLACER
- K810207 — MINOR SURGERY LIGHT
- K802928 — SPIROMETRIC COMPUTER #SC-10
- K801623 — CAVITRON ULTRASONIC SURG. ASPIR. CUSA
- K801877 — SLIT LAMP ATTACHMENT
- K800869 — MODEL PM-20(N)(R)CO2 PATIENT MONITOR/ALA
- K800722 — AUTO-FIELD D AUTOMATED VISUAL DETECTOR
- K791585 — MODEL G-61 ULTRASONIC DENTAL UNIT
- K791277 — MODEL 6500 EXTRACTION IRRIGATION SYS
- K782054 — LASER, CO2 SURGICAL
- K782065 — LASER, PHOTOCOAGULATION
- K781462 — AUTO-FIELD II OPHTHALMIC FIELD SCANNER
- K781014 — AUTOREFRACTOR, SUBJECTIVE
- K781136 — TEMPERATURE MODULE, DUAL
- K780964 — TRANSPORT INCUBATOR
- K780811 — DENTAL ABRASIVE DEVICE
- K780345 — PHOTOCOAGULATOR LASER
- K780162 — DIGAPHOT PHOTOTHERAPY METER MODEL PT 145
- K780046 — ULTRASPHYG BLOOD PRESSURE OPTION
- K780376 — MINIDENTOFLEX NEW POLISHING SYSTEM
- K780377 — PINIDENTOFLEX DENTAL POLISHER
- K771025 — PHOTOTHERAPY/PROCEDURE LAMP
- K771658 — IDENTOFLEX
- K771368 — PORTABLE INFANT VENTILATOR
- K771371 — SCREENING COMPUTEO SC-20
- K771028 — ANALYZER, OXYGEN, MODEL OM-92
- K770969 — CLEV-DENT COLHS ELECTROSURG, MOLEL TR-5
- K770968 — MONITOR, PATIENT, MODEL PM-I0N
- K770736 — MONITOR, PATIENT, MODEL PM-20N
- K770713 — MONITOR, PATIENT, RESP. CARBON DIOXIDE
- K770532 — PC-30 PULMONARY COMPUTER
- K760805 — ULTRASONIC DENTAL PROPHYLAXIS DEVICE
Data sourced from openFDA. This site is unofficial and independent of the FDA.