Pulmonary Data Services Inst., Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Pulmonary Data Services Inst., Inc. makes
Pulmonary Data Services Inst., Inc. manufactures the KOKO FILTER II, a medical device designed for respiratory applications, likely intended to filter or purify inhaled air in clinical or home settings.
The KOKO FILTER II is classified as a Class II device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Koko Legend Ref K051572
Regimes: 510(k) Registry: 510(k)Koko Filter Ii Ref K934475
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Pulmonary Data Services Inst., Inc. have in the registry?
The registry currently lists 2 devices for Pulmonary Data Services Inst., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Pulmonary Data Services Inst., Inc.'s devices?
Among its 2 most recently registered devices, Pulmonary Data Services Inst., Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Pulmonary Data Services Inst., Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Pulmonary Data Services Inst., Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Pulmonary Data Services Inst., Inc. in the registry?
The most recently registered devices listed for Pulmonary Data Services Inst., Inc. include KOKO LEGEND and KOKO FILTER II.