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FDA 510(k)

MODEL P-33, BATTERY OPERATED, THREE WHEEL, POWER SCOOTER , MODEL P-33

K-Number: K020002 · 2002-03-21

Decision Date2002-03-21
Product CodeINI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MODEL P-33, BATTERY OPERATED, THREE WHEEL, POWER SCOOTER , MODEL P-33 is the device name listed in this FDA 510(k) record. The listed applicant is Transworld Mobility Distribution, LLC. It received FDA 510(k) clearance on 2002-03-21 under 510(k) number K020002. 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 MODEL P-33, BATTERY OPERATED, THREE WHEEL, POWER SCOOTER , MODEL P-33?

MODEL P-33, BATTERY OPERATED, THREE WHEEL, POWER SCOOTER , MODEL P-33 is a medical device that received FDA 510(k) clearance on 2002-03-21. The listed applicant is Transworld Mobility Distribution, LLC. The 510(k) number is K020002.

When did MODEL P-33, BATTERY OPERATED, THREE WHEEL, POWER SCOOTER , MODEL P-33 receive FDA 510(k) clearance?

MODEL P-33, BATTERY OPERATED, THREE WHEEL, POWER SCOOTER , MODEL P-33 received FDA 510(k) clearance on 2002-03-21, under 510(k) number K020002.

Who is the listed applicant for MODEL P-33, BATTERY OPERATED, THREE WHEEL, POWER SCOOTER , MODEL P-33?

The FDA 510(k) record lists Transworld Mobility Distribution, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MODEL P-33, BATTERY OPERATED, THREE WHEEL, POWER SCOOTER , MODEL P-33?

The FDA product code for MODEL P-33, BATTERY OPERATED, THREE WHEEL, POWER SCOOTER , MODEL P-33 is INI.

Related Clinical Trials

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.

Other records listing Transworld Mobility Distribution, LLC 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.

Related Devices (Code: INI)

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.

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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