Ahlstrom Nonwovens, LLC is one of 18408 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ahlstrom Nonwovens, LLC - FDA 510(k) Cleared Devices
Recent clearances: Reliance Solo Sterilization Wrap, Reliance Tandem Sterilization Wrap, Reliance Solo Sterilization Wrap, Reliance Tandem Sterilization Wrap
2
Total
2
Cleared
0
Denied
Ahlstrom Nonwovens, LLC has 2 FDA 510(k) cleared medical devices. Based in Windsor Locks, US.
Historical record: 2 cleared submissions from 2016 to 2017. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Ahlstrom Nonwovens, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Ajw Technology Consultants, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Ahlstrom Nonwovens, LLC
2 devices