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Cavitron Corp.

Mchenry, IL, US

Cavitron Corp. appears in FDA device records in Mchenry, IL. FDA records list 32 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.

FDA records held for this company

510(k) clearances
32
PMA records
0
Recall records
0
Registered establishments
0

510(k) clearance history

FDA records hold 32 510(k) clearances for Cavitron Corp. between 1976 and 1981. The busiest year on record is 1978, with 11. The most recent is 1981, with 2.

Clearances by year, as a table
510(k) clearance decisions for Cavitron Corp., by decision year
YearClearances
19761
197710
197811
19793
19805
19812
510(k) clearances on record, most recent first
K numberDeviceProduct codeDecisionDecision date
K811582THE PLACEREIDSubstantially Equivalent
K810207MINOR SURGERY LIGHTGBCSubstantially Equivalent
K802928SPIROMETRIC COMPUTER #SC-10BZCSubstantially Equivalent
K801623CAVITRON ULTRASONIC SURG. ASPIR. CUSALFLSubstantially Equivalent
K801877SLIT LAMP ATTACHMENTHQBSubstantially Equivalent
K800869MODEL PM-20(N)(R)CO2 PATIENT MONITOR/ALACCKSubstantially Equivalent
K800722AUTO-FIELD D AUTOMATED VISUAL DETECTORHPTSubstantially Equivalent
K791585MODEL G-61 ULTRASONIC DENTAL UNITELCSubstantially Equivalent
K791277MODEL 6500 EXTRACTION IRRIGATION SYSHDQSubstantially Equivalent
K782054LASER, CO2 SURGICALHHRSubstantially Equivalent
K782065LASER, PHOTOCOAGULATIONHQFSubstantially Equivalent
K781462AUTO-FIELD II OPHTHALMIC FIELD SCANNERHPTSubstantially Equivalent
K781014AUTOREFRACTOR, SUBJECTIVEHKOSubstantially Equivalent
K781136TEMPERATURE MODULE, DUALFLLSubstantially Equivalent
K780964TRANSPORT INCUBATORFPLSubstantially Equivalent
K780811DENTAL ABRASIVE DEVICEEHLSubstantially Equivalent
K780345PHOTOCOAGULATOR LASERHQBSubstantially Equivalent
K780162DIGAPHOT PHOTOTHERAPY METER MODEL PT 145FTASubstantially Equivalent
K780046ULTRASPHYG BLOOD PRESSURE OPTIONDXNSubstantially Equivalent
K780377PINIDENTOFLEX DENTAL POLISHEREHLSubstantially Equivalent
K780376MINIDENTOFLEX NEW POLISHING SYSTEMEHLSubstantially Equivalent
K771025PHOTOTHERAPY/PROCEDURE LAMPLBISubstantially Equivalent
K771658IDENTOFLEXEHJSubstantially Equivalent
K771371SCREENING COMPUTEO SC-20BZMSubstantially Equivalent
K771368PORTABLE INFANT VENTILATORFOCSubstantially Equivalent
K771028ANALYZER, OXYGEN, MODEL OM-92CCLSubstantially Equivalent
K770969CLEV-DENT COLHS ELECTROSURG, MOLEL TR-5GEISubstantially Equivalent
K770968MONITOR, PATIENT, MODEL PM-I0NCCKSubstantially Equivalent
K770736MONITOR, PATIENT, MODEL PM-20NCHLSubstantially Equivalent
K770713MONITOR, PATIENT, RESP. CARBON DIOXIDECCKSubstantially Equivalent
K770532PC-30 PULMONARY COMPUTERBZCSubstantially Equivalent
K760805ULTRASONIC DENTAL PROPHYLAXIS DEVICEELCSubstantially Equivalent

Registered establishments

No FDA establishment registrations recorded against this company.

FDA product codes

Recall records

No recall records for this company in the ingested FDA data.

Verification record

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Data as of , FDA export datePage updated Source: openFDA, public domain