Central Plastic, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Central Plastic, Inc. makes
Central Plastic, Inc. manufactures disposable and anti-fog IV induction covers, which are designed to protect intravenous insertion sites during medical procedures. These products are intended for single-use applications in clinical settings to reduce contamination risks and improve visibility of the insertion site.
The company’s portfolio includes devices classified as Class I and Class II under FDA regulations, with products listed via the 510(k) clearance pathway. These products are registered and compliant with U.S. medical device regulations, adhering to the requirements for sterile and non-sterile devices in healthcare environments.
Catalogue
Anti-Fog Disposable Iv Induction Cover Ref K910104
Regimes: 510(k) Registry: 510(k)Disposable Iv Induction Cover Ref K894427
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Central Plastic, Inc. have in the registry?
The registry currently lists 2 devices for Central Plastic, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Central Plastic, Inc.'s devices?
Among its 2 most recently registered devices, Central Plastic, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Central Plastic, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Central Plastic, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Central Plastic, Inc. in the registry?
The most recently registered devices listed for Central Plastic, Inc. include ANTI-FOG DISPOSABLE IV INDUCTION COVER and DISPOSABLE IV INDUCTION COVER.