Reliance® Fusion Sterilization Wraps
K-Number: K230137 · 2023-12-07
ApplicantAhlstrom-Munksjo Nonwovens, LLC
Decision Date2023-12-07
Product CodeFRG
Advisory CommitteeHO
DecisionSubstantially Equivalent
Device Summary
Reliance® Fusion Sterilization Wraps is a medical device manufactured by Ahlstrom-Munksjo Nonwovens, LLC. It received FDA 510(k) clearance on 2023-12-07 under approval number K230137. The device is classified under product code FRG. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Reliance® Fusion Sterilization Wraps?
Reliance® Fusion Sterilization Wraps is a medical device that received FDA 510(k) clearance on 2023-12-07. It is manufactured by Ahlstrom-Munksjo Nonwovens, LLC. The 510(k) number is K230137.
When was Reliance® Fusion Sterilization Wraps approved by the FDA?
Reliance® Fusion Sterilization Wraps received FDA 510(k) clearance on 2023-12-07, under approval number K230137.
What company makes Reliance® Fusion Sterilization Wraps?
Reliance® Fusion Sterilization Wraps is manufactured by Ahlstrom-Munksjo Nonwovens, LLC.
What is the FDA product code for Reliance® Fusion Sterilization Wraps?
The FDA product code for Reliance® Fusion Sterilization Wraps is FRG.
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Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.