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FDA 510(k)

MODIFICATION TO MEDLINE STRIDER MIDI 3

K-Number: K042763 · 2004-10-07

ApplicantMedline Industries, Inc.
Decision Date2004-10-07
Product CodeINI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MODIFICATION TO MEDLINE STRIDER MIDI 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 2004-10-07 under 510(k) number K042763. 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 MODIFICATION TO MEDLINE STRIDER MIDI 3?

MODIFICATION TO MEDLINE STRIDER MIDI 3 is a medical device that received FDA 510(k) clearance on 2004-10-07. The listed applicant is Medline Industries, Inc.. The 510(k) number is K042763.

When did MODIFICATION TO MEDLINE STRIDER MIDI 3 receive FDA 510(k) clearance?

MODIFICATION TO MEDLINE STRIDER MIDI 3 received FDA 510(k) clearance on 2004-10-07, under 510(k) number K042763.

Who is the listed applicant for MODIFICATION TO MEDLINE STRIDER MIDI 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 MODIFICATION TO MEDLINE STRIDER MIDI 3?

The FDA product code for MODIFICATION TO MEDLINE STRIDER MIDI 3 is INI.

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Related Devices (Code: 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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