Medical Device Manufacturer · US , Columbus , OH

Pedia Pals, Inc. - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 1991

Total

Cleared

Denied

Pedia Pals, Inc. has 7 FDA 510(k) cleared medical devices. Based in Columbus, US.

Historical record: 7 cleared submissions from 1991 to 1995. Primary specialty: Cardiovascular.

Browse the FDA 510(k) cleared devices submitted by Pedia Pals, Inc. Filter by specialty or product code using the sidebar.

Pedia Pals, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Pedia Pals, Inc.

7 devices

1-7 of 7