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FDA 510(k)

ORLAU SWIVEL WALKER

K-Number: K923880 · 1996-09-30

ApplicantMopac, Ltd.
Decision Date1996-09-30
Product CodeMRI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

ORLAU SWIVEL WALKER is the device name listed in this FDA 510(k) record. The listed applicant is Mopac, Ltd.. It received FDA 510(k) clearance on 1996-09-30 under 510(k) number K923880. The device is classified under product code MRI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ORLAU SWIVEL WALKER?

ORLAU SWIVEL WALKER is a medical device that received FDA 510(k) clearance on 1996-09-30. The listed applicant is Mopac, Ltd.. The 510(k) number is K923880.

When did ORLAU SWIVEL WALKER receive FDA 510(k) clearance?

ORLAU SWIVEL WALKER received FDA 510(k) clearance on 1996-09-30, under 510(k) number K923880.

Who is the listed applicant for ORLAU SWIVEL WALKER?

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

What is the FDA product code for ORLAU SWIVEL WALKER?

The FDA product code for ORLAU SWIVEL WALKER is MRI.

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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.

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