Dytek Corp.
United StatesFDA 510(k) applicant, unverified
- Devices
- 3
Catalogue
Pencil, Electrosurgical Ref K760168
510(k) 510(k)Bag, Post Operative Lung Exercizing Blow Ref K760167
510(k) 510(k)Lung Exer. Bag, Post-Op, Modified Ref K781245
510(k) 510(k)
Frequently asked questions
How many devices does Dytek Corp. have in the registry?
The registry currently lists 3 devices for Dytek Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Dytek Corp.'s devices?
Among its 3 most recently registered devices, Dytek Corp. has devices listed in FDA 510(k) (3 devices).
What risk classes do Dytek Corp.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Dytek Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Dytek Corp. in the registry?
The most recently registered devices listed for Dytek Corp. include PENCIL, ELECTROSURGICAL, BAG, POST OPERATIVE LUNG EXERCIZING BLOW and LUNG EXER. BAG, POST-OP, MODIFIED.