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FDA 510(k)

Medline Reusable Sterilization Wrappers

K-Number: K234132 · 2024-09-17

ApplicantMedline Industries, LP
Decision Date2024-09-17
Product CodeFRG
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

Medline Reusable Sterilization Wrappers is a medical device manufactured by Medline Industries, LP. It received FDA 510(k) clearance on 2024-09-17 under approval number K234132. 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 Medline Reusable Sterilization Wrappers?

Medline Reusable Sterilization Wrappers is a medical device that received FDA 510(k) clearance on 2024-09-17. It is manufactured by Medline Industries, LP. The 510(k) number is K234132.

When was Medline Reusable Sterilization Wrappers approved by the FDA?

Medline Reusable Sterilization Wrappers received FDA 510(k) clearance on 2024-09-17, under approval number K234132.

What company makes Medline Reusable Sterilization Wrappers?

Medline Reusable Sterilization Wrappers is manufactured by Medline Industries, LP.

What is the FDA product code for Medline Reusable Sterilization Wrappers?

The FDA product code for Medline Reusable Sterilization Wrappers 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.

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