FDA 510(k)

MEDLINE STERILIZATION WRAP

K-Number: K002968 · 2001-01-23

Decision Date2001-01-23

Product CodeFRG

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

MEDLINE STERILIZATION WRAP is the device name listed in this FDA 510(k) record. The listed applicant is Medline Industries, Inc.. It received FDA 510(k) clearance on 2001-01-23 under 510(k) number K002968. 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 STERILIZATION WRAP?

MEDLINE STERILIZATION WRAP is a medical device that received FDA 510(k) clearance on 2001-01-23. The listed applicant is Medline Industries, Inc.. The 510(k) number is K002968.

When did MEDLINE STERILIZATION WRAP receive FDA 510(k) clearance?

MEDLINE STERILIZATION WRAP received FDA 510(k) clearance on 2001-01-23, under 510(k) number K002968.

Who is the listed applicant for MEDLINE STERILIZATION WRAP?

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

What is the FDA product code for MEDLINE STERILIZATION WRAP?

The FDA product code for MEDLINE STERILIZATION WRAP 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.