Rsp, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Rsp, Inc. makes
Rsp, Inc. manufactures an esophageal stethoscope, a device used for auscultation of the esophagus, and epidural catheters, which are inserted into the epidural space for medication delivery or diagnostic procedures.
The company’s products are regulated under the FDA’s Class I and Class II categories and are listed in the 510(k) clearance registry. The manufacturer is based in the United States.
Catalogue
Esophageal Stethoscope Ref K823703
Regimes: 510(k) Registry: 510(k)Epidural Catheter Ref K823702
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Rsp, Inc. have in the registry?
The registry currently lists 2 devices for Rsp, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Rsp, Inc.'s devices?
Among its 2 most recently registered devices, Rsp, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Rsp, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Rsp, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Rsp, Inc. in the registry?
The most recently registered devices listed for Rsp, Inc. include ESOPHAGEAL STETHOSCOPE and EPIDURAL CATHETER.