Medical Device Manufacturer · JP , Tokyo

Pigeon Corp. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1994
2
Total
2
Cleared
0
Denied

Pigeon Corp. has 2 FDA 510(k) cleared medical devices. Based in Tokyo, JP.

Historical record: 2 cleared submissions from 1994 to 1994. Primary specialty: Obstetrics & Gynecology.

Browse the FDA 510(k) cleared devices submitted by Pigeon Corp. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Pigeon Corp.

2 devices
1-2 of 2
Filters