Diversatronics, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Diversatronics, Inc. makes
Diversatronics, Inc. manufactures sterile adhesive labels for medical packaging, a pneumatic device for maintaining anterior chamber pressure during ophthalmic procedures, and a nebulizer system for pharmaceutical aerosol delivery.
The company’s products are regulated as Class II medical devices in the US and are listed under 510(k) premarket notifications with the FDA. Diversatronics, Inc. is based in the United States.
Catalogue
Sterilabels Ref K864015
Regimes: 510(k) Registry: 510(k)Pneumatic Anterior Chamber Maintainer Ref K830143
Regimes: 510(k) Registry: 510(k)Pharmatronics Nebulizer Ref K896536
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Diversatronics, Inc. have in the registry?
The registry currently lists 3 devices for Diversatronics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Diversatronics, Inc.'s devices?
Among its 3 most recently registered devices, Diversatronics, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Diversatronics, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Diversatronics, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Diversatronics, Inc. in the registry?
The most recently registered devices listed for Diversatronics, Inc. include STERILABELS, PNEUMATIC ANTERIOR CHAMBER MAINTAINER and PHARMATRONICS NEBULIZER.