Omnitron Intl., Inc.
Omnitron Intl., Inc. holds FDA 510(k) medical device clearances, first cleared 1988, most recent 1992.
Top product codes for Omnitron Intl., Inc.
Recent clearances by Omnitron Intl., Inc.
- K901615 — PULMOCATH INTRABRONCHIAL CATHETER
- K923130 — IR-192 IMPLANT -- MODIFICATION
- K920431 — OMNITRON NEEDLE APPLICATORS 18 AND 21 GAUGE
- K913908 — OMNITRON GYN APPLICATOR SYSTEM
- K915253 — IR-192 IMPLANT, MODIFICATION
- K911775 — OMNICATH IMPLANTED CATHETER AND DEPOT
- K881665 — OMNITRON REMOTE CONTROLLED RADIONUCLIDE APPLICATOR
Data sourced from openFDA. This site is unofficial and independent of the FDA.