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FDA 510(k)

MEDLINE STRIDER MAXI 3

K-Number: K041054 · 2004-05-25

ApplicantMedline Industries, Inc.
Decision Date2004-05-25
Product CodeINI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MEDLINE STRIDER MAXI 3 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 2004-05-25 under 510(k) number K041054. The device is classified under product code INI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDLINE STRIDER MAXI 3?

MEDLINE STRIDER MAXI 3 is a medical device that received FDA 510(k) clearance on 2004-05-25. The listed applicant is Medline Industries, Inc.. The 510(k) number is K041054.

When did MEDLINE STRIDER MAXI 3 receive FDA 510(k) clearance?

MEDLINE STRIDER MAXI 3 received FDA 510(k) clearance on 2004-05-25, under 510(k) number K041054.

Who is the listed applicant for MEDLINE STRIDER MAXI 3?

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 STRIDER MAXI 3?

The FDA product code for MEDLINE STRIDER MAXI 3 is INI.

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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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