Whiteline Plastics, Inc.
CanadaFDA applicant, unverified
- Devices
- 1
What Whiteline Plastics, Inc. makes
Whiteline Plastics, Inc. manufactures the Face-2-Face CPR Protection Shield, a barrier device designed to prevent direct contact between rescuers and patients during cardiopulmonary resuscitation (CPR). This product is intended to reduce exposure risks while maintaining the effectiveness of chest compressions.
The company’s portfolio is regulated under Class II medical devices in the United States, with the Face-2-Face CPR Protection Shield listed via the FDA’s 510(k) clearance pathway. The manufacturer operates from the United States.
Catalogue
Face-2-Face Cpr Protection Shield Ref K991617
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Whiteline Plastics, Inc. have in the registry?
The registry currently lists 1 device for Whiteline Plastics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Whiteline Plastics, Inc.'s devices?
Among its 1 most recently registered device, Whiteline Plastics, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Whiteline Plastics, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Whiteline Plastics, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Whiteline Plastics, Inc. in the registry?
The most recently registered devices listed for Whiteline Plastics, Inc. include FACE-2-FACE CPR PROTECTION SHIELD.