Ann Arbor Plastics, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Ann Arbor Plastics, Inc. makes
Ann Arbor Plastics, Inc. manufactures medium-sized oxygen hoods, including model #1547, designed for controlled oxygen delivery in medical settings.
These devices are classified as Class I under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Medium Size Oxygen Hood #1547 Ref K802653
Regimes: 510(k) Registry: 510(k)Oxygen Hoods Ref K791861
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ann Arbor Plastics, Inc. have in the registry?
The registry currently lists 2 devices for Ann Arbor Plastics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ann Arbor Plastics, Inc.'s devices?
Among its 2 most recently registered devices, Ann Arbor Plastics, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Ann Arbor Plastics, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Ann Arbor Plastics, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Ann Arbor Plastics, Inc. in the registry?
The most recently registered devices listed for Ann Arbor Plastics, Inc. include MEDIUM SIZE OXYGEN HOOD #1547 and OXYGEN HOODS.