Ppg/Applied Resources, Inc.
United StatesFDA applicant, unverified
- Devices
- 5
What Ppg/Applied Resources, Inc. makes
Ppg/Applied Resources, Inc. manufactures surgical and monitoring devices for anesthesia and patient ventilation, including the O.R. SARACAP (a capnograph for measuring exhaled CO₂), SARA AGIE MONITOR (a ventilator monitoring system), SARACAP AG (a portable capnograph), SARA DIGICAP (a digital capnography system), and ICU SARACAP (a capnograph for intensive care settings). These devices are designed to support respiratory monitoring and capnography in operating rooms and critical care environments.
The company’s products are classified as Class II medical devices under FDA regulations and are listed via the 510(k) clearance process. The portfolio is regulated in the United States, where the manufacturer is based.
Catalogue
O.R. Saracap Ref K881002
Regimes: 510(k) Registry: 510(k)Sara Agie Monitor Ref K874724
Regimes: 510(k) Registry: 510(k)Saracap AG Ref K882172
Regimes: 510(k) Registry: 510(k)Sara Digicap Ref K874754
Regimes: 510(k) Registry: 510(k)Icu Saracap Ref K881093
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ppg/Applied Resources, Inc. have in the registry?
The registry currently lists 5 devices for Ppg/Applied Resources, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ppg/Applied Resources, Inc.'s devices?
Among its 5 most recently registered devices, Ppg/Applied Resources, Inc. has devices listed in FDA 510(k) (5 devices).
What risk classes do Ppg/Applied Resources, Inc.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for Ppg/Applied Resources, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Ppg/Applied Resources, Inc. in the registry?
The most recently registered devices listed for Ppg/Applied Resources, Inc. include O.R. SARACAP, SARA AGIE MONITOR, SARACAP AG and SARA DIGICAP.