Micro-Pap Corp.
Country not established
- Devices
- 1
What Micro-Pap Corp. makes
Micro-Pap Corp. manufactures the MICRO-PAP™ Kit, a medical device designed for specific clinical applications in respiratory or pulmonary diagnostics.
The MICRO-PAP™ Kit is classified as a Class II device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Micro-Pap(Tm) Kit Ref K912325
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Micro-Pap Corp. have in the registry?
The registry currently lists 1 device for Micro-Pap Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Micro-Pap Corp.'s devices?
Among its 1 most recently registered device, Micro-Pap Corp. has devices listed in FDA 510(k) (1 device).
What risk classes do Micro-Pap Corp.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Micro-Pap Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Micro-Pap Corp. in the registry?
The most recently registered devices listed for Micro-Pap Corp. include MICRO-PAP(TM) KIT.