Viratest Intl., Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Viratest Intl., Inc. makes
Viratest Intl., Inc. manufactures diagnostic transport devices, including the DIADOT™ Virus/Chlamydia Transport, designed for the collection and preservation of specimens for laboratory testing. The company also produces cell culture products, such as the A549 Cell Culture and MRC-5 Cell Culture Vial, used for research and testing purposes in vitro.
These products are classified as Class I medical devices under FDA regulations and are listed in the 510(k) clearance database. The company is based in the United States.
Catalogue
Diadot(Tm) Virus/Chlamydia Transport Ref K931922
Regimes: 510(k) Registry: 510(k)A549 Cell Culture Ref K955921
Regimes: 510(k) Registry: 510(k)Mrc-5 Cell Culture Vial Ref K952727
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Viratest Intl., Inc. have in the registry?
The registry currently lists 3 devices for Viratest Intl., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Viratest Intl., Inc.'s devices?
Among its 3 most recently registered devices, Viratest Intl., Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Viratest Intl., Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Viratest Intl., Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Viratest Intl., Inc. in the registry?
The most recently registered devices listed for Viratest Intl., Inc. include DIADOT(TM) VIRUS/CHLAMYDIA TRANSPORT, A549 CELL CULTURE and MRC-5 CELL CULTURE VIAL.