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FDA 510(k)

ACTIVA

K-Number: K991132 · 1999-10-20

ApplicantHoveround Corp.
Decision Date1999-10-20
Product CodeINI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

ACTIVA is the device name listed in this FDA 510(k) record. The listed applicant is Hoveround Corp.. It received FDA 510(k) clearance on 1999-10-20 under 510(k) number K991132. 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 ACTIVA?

ACTIVA is a medical device that received FDA 510(k) clearance on 1999-10-20. The listed applicant is Hoveround Corp.. The 510(k) number is K991132.

When did ACTIVA receive FDA 510(k) clearance?

ACTIVA received FDA 510(k) clearance on 1999-10-20, under 510(k) number K991132.

Who is the listed applicant for ACTIVA?

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 ACTIVA?

The FDA product code for ACTIVA is INI.

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Other records listing Hoveround Corp. as applicant

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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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