Vitalab Products Corp.
United StatesFDA 510(k) applicant, unverified
- Devices
- 4
Catalogue
Mask, Pxygen Ref K781413
510(k) 510(k)Tubing, Flexible, Medical Gas Ref K781416
510(k) 510(k)Mask, Oxygen, Nonbreathing Ref K781414
510(k) 510(k)Cannula, Nasal, Oxygen Ref K781415
510(k) 510(k)
Frequently asked questions
How many devices does Vitalab Products Corp. have in the registry?
The registry currently lists 4 devices for Vitalab Products Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Vitalab Products Corp.'s devices?
Among its 4 most recently registered devices, Vitalab Products Corp. has devices listed in FDA 510(k) (4 devices).
What risk classes do Vitalab Products Corp.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Vitalab Products Corp.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Vitalab Products Corp. in the registry?
The most recently registered devices listed for Vitalab Products Corp. include MASK, PXYGEN, TUBING, FLEXIBLE, MEDICAL GAS, MASK, OXYGEN, NONBREATHING and CANNULA, NASAL, OXYGEN.