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FDA 510(k)

LA PERSONAL SCOOTER

K-Number: K000869 · 2000-07-19

ApplicantAssembled Products Corp.
Decision Date2000-07-19
Product CodeINI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

LA PERSONAL SCOOTER is the device name listed in this FDA 510(k) record. The listed applicant is Assembled Products Corp.. It received FDA 510(k) clearance on 2000-07-19 under 510(k) number K000869. 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 LA PERSONAL SCOOTER?

LA PERSONAL SCOOTER is a medical device that received FDA 510(k) clearance on 2000-07-19. The listed applicant is Assembled Products Corp.. The 510(k) number is K000869.

When did LA PERSONAL SCOOTER receive FDA 510(k) clearance?

LA PERSONAL SCOOTER received FDA 510(k) clearance on 2000-07-19, under 510(k) number K000869.

Who is the listed applicant for LA PERSONAL SCOOTER?

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

What is the FDA product code for LA PERSONAL SCOOTER?

The FDA product code for LA PERSONAL SCOOTER is 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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