Esp Plastics, Inc.
United StatesFDA applicant, unverified
- Devices
- 4
What Esp Plastics, Inc. makes
Esp Plastics, Inc. manufactures single-use respiratory and anesthesia devices, including breathing circuits with access ports, Guedel oropharyngeal airways, bacterial filters for anesthesia circuits, and manual breathing bags.
The company’s products are regulated under FDA’s Class I and Class II classifications, with most devices authorised via the 510(k) pathway. They are listed in the FDA’s 510(k) database and are based in the United States.
Catalogue
Espree' Breathing Circuit (W/Access Ref K821311
Regimes: 510(k) Registry: 510(k)Espree' Guedel Espree Berman Airway Ref K821308
Regimes: 510(k) Registry: 510(k)Espree' Anesthesia Bacterial Filter Ref K821310
Regimes: 510(k) Registry: 510(k)Espree', Breathing Bag Ref K821309
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Esp Plastics, Inc. have in the registry?
The registry currently lists 4 devices for Esp Plastics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Esp Plastics, Inc.'s devices?
Among its 4 most recently registered devices, Esp Plastics, Inc. has devices listed in FDA 510(k) (4 devices).
What risk classes do Esp Plastics, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Esp Plastics, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Esp Plastics, Inc. in the registry?
The most recently registered devices listed for Esp Plastics, Inc. include ESPREE' BREATHING CIRCUIT (W/ACCESS, ESPREE' GUEDEL ESPREE BERMAN AIRWAY, ESPREE' ANESTHESIA BACTERIAL FILTER and ESPREE', BREATHING BAG.