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FDA 510(k)

HOVEROUND MPV

K-Number: K935410 · 1994-03-28

ApplicantHoveround Corp.
Decision Date1994-03-28
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent for Some Indications

Device Summary

HOVEROUND MPV is the device name listed in this FDA 510(k) record. The listed applicant is Hoveround Corp.. It received FDA 510(k) clearance on 1994-03-28 under 510(k) number K935410. The device is classified under product code ITI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the HOVEROUND MPV?

HOVEROUND MPV is a medical device that received FDA 510(k) clearance on 1994-03-28. The listed applicant is Hoveround Corp.. The 510(k) number is K935410.

When did HOVEROUND MPV receive FDA 510(k) clearance?

HOVEROUND MPV received FDA 510(k) clearance on 1994-03-28, under 510(k) number K935410.

Who is the listed applicant for HOVEROUND MPV?

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

What is the FDA product code for HOVEROUND MPV?

The FDA product code for HOVEROUND MPV is ITI.

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Other records listing Hoveround Corp. 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.

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Related Devices (Code: ITI)

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.

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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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