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FDA 510(k)

Medicom Sterilization Wrap

K-Number: K240862 · 2024-06-21

Decision Date2024-06-21
Product CodeFRG
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

Medicom Sterilization Wrap is the device name listed in this FDA 510(k) record. The listed applicant is Medicom Group, Inc.. It received FDA 510(k) clearance on 2024-06-21 under 510(k) number K240862. 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 Medicom Sterilization Wrap?

Medicom Sterilization Wrap is a medical device that received FDA 510(k) clearance on 2024-06-21. The listed applicant is Medicom Group, Inc.. The 510(k) number is K240862.

When did Medicom Sterilization Wrap receive FDA 510(k) clearance?

Medicom Sterilization Wrap received FDA 510(k) clearance on 2024-06-21, under 510(k) number K240862.

Who is the listed applicant for Medicom Sterilization Wrap?

The FDA 510(k) record lists Medicom Group, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Medicom Sterilization Wrap?

The FDA product code for Medicom Sterilization Wrap 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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