Cavitron Corp.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
32
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K811582THE PLACERJuly 28, 1981
K810207MINOR SURGERY LIGHTFebruary 13, 1981
K802928SPIROMETRIC COMPUTER #SC-10December 17, 1980
K801623CAVITRON ULTRASONIC SURG. ASPIR. CUSANovember 18, 1980
K801877SLIT LAMP ATTACHMENTSeptember 16, 1980
K800869MODEL PM-20(N)(R)CO2 PATIENT MONITOR/ALAMay 28, 1980
K800722AUTO-FIELD D AUTOMATED VISUAL DETECTORApril 29, 1980
K791585MODEL G-61 ULTRASONIC DENTAL UNITSeptember 19, 1979
K791277MODEL 6500 EXTRACTION IRRIGATION SYSAugust 22, 1979
K782054LASER, CO2 SURGICALJanuary 17, 1979
K782065LASER, PHOTOCOAGULATIONDecember 28, 1978
K781462AUTO-FIELD II OPHTHALMIC FIELD SCANNERSeptember 14, 1978
K781014AUTOREFRACTOR, SUBJECTIVESeptember 7, 1978
K781136TEMPERATURE MODULE, DUALAugust 10, 1978
K780964TRANSPORT INCUBATORJuly 27, 1978
K780811DENTAL ABRASIVE DEVICEJune 22, 1978
K780345PHOTOCOAGULATOR LASERMay 9, 1978
K780162DIGAPHOT PHOTOTHERAPY METER MODEL PT 145March 27, 1978
K780046ULTRASPHYG BLOOD PRESSURE OPTIONMarch 15, 1978
K780377PINIDENTOFLEX DENTAL POLISHERMarch 14, 1978