Pigeon Corp.
JapanFDA applicant, unverified
- Devices
- 2
What Pigeon Corp. makes
Pigeon Corp. manufactures breast pumps, including the Advanced MagMag AC/Battery Breast Pump and the Deluxe MagMag Breast Pump.
These devices are classified as Class II medical devices and are listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
Advanced Magmag Ac/Battery Breast Pump Ref K935249
Regimes: 510(k) Registry: 510(k)Deluxe Magmag Breast Pump Ref K936309
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Pigeon Corp. have in the registry?
The registry currently lists 2 devices for Pigeon Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Pigeon Corp.'s devices?
Among its 2 most recently registered devices, Pigeon Corp. has devices listed in FDA 510(k) (2 devices).
What risk classes do Pigeon Corp.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Pigeon Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Pigeon Corp. in the registry?
The most recently registered devices listed for Pigeon Corp. include ADVANCED MAGMAG AC/BATTERY BREAST PUMP and DELUXE MAGMAG BREAST PUMP.