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Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account

Cavitron Corp. — Predicate Candidate Screening

32 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.

33 daysmedian FDA review time
69 days90th percentile
32clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K811582THE PLACERCavitron Corp.1981-07-28530
K810207MINOR SURGERY LIGHTCavitron Corp.1981-02-13180
K802928SPIROMETRIC COMPUTER #SC-10Cavitron Corp.1980-12-17280
K801623CAVITRON ULTRASONIC SURG. ASPIR. CUSACavitron Corp.1980-11-181260
K801877SLIT LAMP ATTACHMENTCavitron Corp.1980-09-16410
K800869MODEL PM-20(N)(R)CO2 PATIENT MONITOR/ALACavitron Corp.1980-05-28410
K800722AUTO-FIELD D AUTOMATED VISUAL DETECTORCavitron Corp.1980-04-29280
K791585MODEL G-61 ULTRASONIC DENTAL UNITCavitron Corp.1979-09-19330
K791277MODEL 6500 EXTRACTION IRRIGATION SYSCavitron Corp.1979-08-22430
K782054LASER, CO2 SURGICALCavitron Corp.1979-01-17410
K782065LASER, PHOTOCOAGULATIONCavitron Corp.1978-12-28150
K781462AUTO-FIELD II OPHTHALMIC FIELD SCANNERCavitron Corp.1978-09-14200
K781014AUTOREFRACTOR, SUBJECTIVECavitron Corp.1978-09-07830
K781136TEMPERATURE MODULE, DUALCavitron Corp.1978-08-10340
K780964TRANSPORT INCUBATORCavitron Corp.1978-07-27450
K780811DENTAL ABRASIVE DEVICECavitron Corp.1978-06-22350
K780345PHOTOCOAGULATOR LASERCavitron Corp.1978-05-09690
K780162DIGAPHOT PHOTOTHERAPY METER MODEL PT 145Cavitron Corp.1978-03-27550
K780046ULTRASPHYG BLOOD PRESSURE OPTIONCavitron Corp.1978-03-15650
K780376MINIDENTOFLEX NEW POLISHING SYSTEMCavitron Corp.1978-03-1460
K780377PINIDENTOFLEX DENTAL POLISHERCavitron Corp.1978-03-1460
K771025PHOTOTHERAPY/PROCEDURE LAMPCavitron Corp.1977-10-251390
K771658IDENTOFLEXCavitron Corp.1977-09-12130
K771368PORTABLE INFANT VENTILATORCavitron Corp.1977-08-04100
K771371SCREENING COMPUTEO SC-20Cavitron Corp.1977-08-04100
K771028ANALYZER, OXYGEN, MODEL OM-92Cavitron Corp.1977-07-05260
K770969CLEV-DENT COLHS ELECTROSURG, MOLEL TR-5Cavitron Corp.1977-06-24240
K770968MONITOR, PATIENT, MODEL PM-I0NCavitron Corp.1977-06-0880
K770736MONITOR, PATIENT, MODEL PM-20NCavitron Corp.1977-06-02420
K770713MONITOR, PATIENT, RESP. CARBON DIOXIDECavitron Corp.1977-04-2790
K770532PC-30 PULMONARY COMPUTERCavitron Corp.1977-04-05150
K760805ULTRASONIC DENTAL PROPHYLAXIS DEVICECavitron Corp.1976-10-2190

Methodology

Recall counts reflect FDA recall records explicitly referencing each K-number; FDA links recalls to K-numbers inconsistently, so 0 means "none found in FDA records," not "never recalled." Data: FDA openFDA, refreshed weekly. Verify decisions of consequence against the primary source. Full candidate set and CSV export: atlasbyauro.com.

Prepared with Atlas

Predicate research, review-time statistics and recall monitoring for 510(k) teams — atlasbyauro.com/fda