Ahlstrom-Munksjo Nonwovens, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ahlstrom-Munksjo Nonwovens, LLC - FDA 510(k) Cleared Devices
Recent clearances: Reliance® Fusion Sterilization Wraps
1
Total
1
Cleared
0
Denied
Ahlstrom-Munksjo Nonwovens, LLC has 1 FDA 510(k) cleared medical devices. Based in Windsor Locks, US.
Last cleared in 2023. Active since 2023. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Ahlstrom-Munksjo 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-Munksjo Nonwovens, LLC
1 devices