Precision Fabrics Group, Inc. is one of 19478 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Precision Fabrics Group, Inc. - FDA 510(k) Cleared Devices
Recent clearances: DermaTherapy Bed Linens, DERMATHERAPY, MODEL 22216
2
Total
2
Cleared
0
Denied
Precision Fabrics Group, Inc. has 2 FDA 510(k) cleared medical devices. Based in Norfolk, US.
Historical record: 2 cleared submissions from 2007 to 2016. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Precision Fabrics Group, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Hogan Lovells US LLP as regulatory consultant.
FDA 510(k) Regulatory Record - Precision Fabrics Group, Inc.
2 devices