Medical Device Manufacturer · US , Grand Junction , CO

Pro-Safe Professional Linens, Inc. - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 1989

Total

Cleared

Denied

Pro-Safe Professional Linens, Inc. has 7 FDA 510(k) cleared medical devices. Based in Grand Junction, US.

Historical record: 7 cleared submissions from 1989 to 1989. Primary specialty: General Hospital.

Browse the FDA 510(k) cleared devices submitted by Pro-Safe Professional Linens, Inc. Filter by specialty or product code using the sidebar.

Pro-Safe Professional Linens, 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 - Pro-Safe Professional Linens, Inc.

7 devices

1-7 of 7