M. Imonti and Associates Inc.,
United StatesFDA 510(k) applicant, unverified
- Devices
- 6
Catalogue
Phacofragmentor Tip Ref K933627
510(k) 510(k)Pro-Pak For Oms Diplomate Ref K950800
510(k) 510(k)Pro-Phaco Handpiece Ref K933503
510(k) 510(k)Pro-Vit Ref K950799
510(k) 510(k)Drainage Tube Restraint/Wound Cover Ref K905766
510(k) 510(k)Endo Trachea Tube Fixation Ref K924551
510(k) 510(k)
Frequently asked questions
How many devices does M. Imonti and Associates Inc., have in the registry?
The registry currently lists 6 devices for M. Imonti and Associates Inc.,. Devices recorded under merged duplicate company entries are counted once.
Which registries list M. Imonti and Associates Inc.,'s devices?
Among its 6 most recently registered devices, M. Imonti and Associates Inc., has devices listed in FDA 510(k) (6 devices).
What risk classes do M. Imonti and Associates Inc.,'s devices fall under?
Among its 6 most recently registered devices, the classes recorded for M. Imonti and Associates Inc.,'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from M. Imonti and Associates Inc., in the registry?
The most recently registered devices listed for M. Imonti and Associates Inc., include PHACOFRAGMENTOR TIP, PRO-PAK FOR OMS DIPLOMATE, PRO-PHACO HANDPIECE and PRO-VIT.