Medline Reusable Sterilization Wrappers
K-Number: K234132 · 2024-09-17
Device Summary
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. The listed applicant is Medline Industries, LP. The 510(k) number is K234132.
When did Medline Reusable Sterilization Wrappers receive FDA 510(k) clearance?
Medline Reusable Sterilization Wrappers received FDA 510(k) clearance on 2024-09-17, under 510(k) number K234132.
Who is the listed applicant for Medline Reusable Sterilization Wrappers?
The FDA 510(k) record lists Medline Industries, LP as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Medline Reusable Sterilization Wrappers?
The FDA product code for Medline Reusable Sterilization Wrappers is FRG.
Other records listing Medline Industries, LP 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.
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.