Pegasus Medical Supply, Inc.
TaiwanFDA 510(k) applicant, unverified
- Devices
- 16
What Pegasus Medical Supply, Inc. makes
Pegasus Medical Supply, Inc. manufactures venous thromboembolism (VTE) prevention devices, including the ANGIO-PRESS LITE and the ANGIO-PRESS DVT Compression Device (Model IPCS), designed for intermittent pneumatic compression therapy.
These devices are classified as Class II under FDA regulations and are listed in the FDA’s 510(k) registry. The company is based in the United States.
Catalogue
Search and filter all 16 devicesCompany details
- DUNS number
- 656766271
Frequently asked questions
How many devices does PEGASUS MEDICAL SUPPLY, INC. have in the registry?
The registry currently lists 16 devices for PEGASUS MEDICAL SUPPLY, INC.. Devices recorded under merged duplicate company entries are counted once.
Which registries list PEGASUS MEDICAL SUPPLY, INC.'s devices?
Among its 16 most recently registered devices, PEGASUS MEDICAL SUPPLY, INC. has devices listed in FDA 510(k) (2 devices) and FDA GUDID (14 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do PEGASUS MEDICAL SUPPLY, INC.'s devices fall under?
Among its 16 most recently registered devices, the classes recorded for PEGASUS MEDICAL SUPPLY, INC.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from PEGASUS MEDICAL SUPPLY, INC. in the registry?
The most recently registered devices listed for PEGASUS MEDICAL SUPPLY, INC. include BluFlex BLU640CB, BluFlex M6, BluFlex BLU660TL and BluFlex BLU610.