Medical Device Manufacturer · US , Mchenry , IL

Megaplast, Inc. - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 1981

Total

Cleared

Denied

Megaplast, Inc. has 7 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 7 cleared submissions from 1981 to 1982. Primary specialty: Gastroenterology & Urology.

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

Megaplast, 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 - Megaplast, Inc.

7 devices

1-7 of 7