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FDA 510(k)

FORMULA IV ELECTRIC MOBILITY VEHICLE

K-Number: K954378 · 1996-07-25

ApplicantAerotek
Decision Date1996-07-25
Product CodeINI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

FORMULA IV ELECTRIC MOBILITY VEHICLE is the device name listed in this FDA 510(k) record. The listed applicant is Aerotek. It received FDA 510(k) clearance on 1996-07-25 under 510(k) number K954378. 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 FORMULA IV ELECTRIC MOBILITY VEHICLE?

FORMULA IV ELECTRIC MOBILITY VEHICLE is a medical device that received FDA 510(k) clearance on 1996-07-25. The listed applicant is Aerotek. The 510(k) number is K954378.

When did FORMULA IV ELECTRIC MOBILITY VEHICLE receive FDA 510(k) clearance?

FORMULA IV ELECTRIC MOBILITY VEHICLE received FDA 510(k) clearance on 1996-07-25, under 510(k) number K954378.

Who is the listed applicant for FORMULA IV ELECTRIC MOBILITY VEHICLE?

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

What is the FDA product code for FORMULA IV ELECTRIC MOBILITY VEHICLE?

The FDA product code for FORMULA IV ELECTRIC MOBILITY VEHICLE is INI.

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Related Devices (Code: INI)

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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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