# Omnitron Intl., Inc.

- Location (FDA's records): Lajke Charles, LA
- FDA decisions: 7 (1988–1992): 7 510(k) clearances
- Product codes: JAQ (4), KXK (2), IWA (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 4 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Varian Assoc., Inc.: 2 (https://510kreport.com/company/varian-assoc)
- Mick Radio-Nuclear Instruments, Inc.: 1 (https://510kreport.com/company/mick-radio-nuclear-instruments)
- Alpha-Omega Services, Inc.: 1 (https://510kreport.com/company/alpha-omega-services)

## Its most-cited devices
- K913908: Omnitron Gyn Applicator System (1992), cited by 2
- K881665: Omnitron Remote Controlled Radionuclide Applicator (1988), cited by 1
- K901615: Pulmocath Intrabronchial Catheter (1992), cited by 1

## Recent decisions
- K901615: Pulmocath Intrabronchial Catheter (Nov 27, 1992)
- K923130: IR-192 Implant -- Modification (Sep 21, 1992)
- K920431: Omnitron Needle Applicators 18 and 21 Gauge (May 29, 1992)
- K913908: Omnitron Gyn Applicator System (Mar 6, 1992)
- K915253: IR-192 Implant, Modification (Feb 27, 1992)
- K911775: Omnicath Implanted Catheter and Depot (May 8, 1991)
- K881665: Omnitron Remote Controlled Radionuclide Applicator (Aug 11, 1988)

Source page: https://510kreport.com/company/omnitron-intl