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FDA 510(k)

Cardinal Health Sterilization Wrap

K-Number: K181174 · 2018-12-11

Decision Date2018-12-11
Product CodeFRG
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

Cardinal Health Sterilization Wrap is the device name listed in this FDA 510(k) record. The listed applicant is Cardinal Health200, LLC. It received FDA 510(k) clearance on 2018-12-11 under 510(k) number K181174. 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 Cardinal Health Sterilization Wrap?

Cardinal Health Sterilization Wrap is a medical device that received FDA 510(k) clearance on 2018-12-11. The listed applicant is Cardinal Health200, LLC. The 510(k) number is K181174.

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

Cardinal Health Sterilization Wrap received FDA 510(k) clearance on 2018-12-11, under 510(k) number K181174.

Who is the listed applicant for Cardinal Health Sterilization Wrap?

The FDA 510(k) record lists Cardinal Health200, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Cardinal Health Sterilization Wrap?

The FDA product code for Cardinal Health Sterilization Wrap is FRG.

Other records listing Cardinal Health200, LLC as applicant

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.

View all 14 devices →

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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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.