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Omnitron Intl., Inc.

7 FDA 510(k) clearances · Manufacturer

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RecordFirmDate
PULMOCATH INTRABRONCHIAL CATHETER (K901615)Omnitron Intl., Inc.1992-11-27
IR-192 IMPLANT -- MODIFICATION (K923130)Omnitron Intl., Inc.1992-09-21
OMNITRON NEEDLE APPLICATORS 18 AND 21 GAUGE (K920431)Omnitron Intl., Inc.1992-05-29
OMNITRON GYN APPLICATOR SYSTEM (K913908)Omnitron Intl., Inc.1992-03-06
IR-192 IMPLANT, MODIFICATION (K915253)Omnitron Intl., Inc.1992-02-27
OMNICATH IMPLANTED CATHETER AND DEPOT (K911775)Omnitron Intl., Inc.1991-05-08
OMNITRON REMOTE CONTROLLED RADIONUCLIDE APPLICATOR (K881665)Omnitron Intl., Inc.1988-08-11

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Every clearance here is in the API, with alerts when new ones post.