Reliance® Fusion Sterilization Wraps
K-Number: K230137 · 2023-12-07
Device Summary
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. The listed applicant is Ahlstrom-Munksjo Nonwovens, LLC. The 510(k) number is K230137.
When did Reliance® Fusion Sterilization Wraps receive FDA 510(k) clearance?
Reliance® Fusion Sterilization Wraps received FDA 510(k) clearance on 2023-12-07, under 510(k) number K230137.
Who is the listed applicant for Reliance® Fusion Sterilization Wraps?
The FDA 510(k) record lists Ahlstrom-Munksjo Nonwovens, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Reliance® Fusion Sterilization Wraps?
The FDA product code for Reliance® Fusion Sterilization Wraps is FRG.
Related Devices (Code: FRG)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
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