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FDA 510(k)

TRAVEL EASE ELECTRIC SCOOTER, MODEL PIONEER 5

K-Number: K013788 · 2001-12-11

ApplicantMerits Health Products Co., Ltd.
Decision Date2001-12-11
Product CodeINI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

TRAVEL EASE ELECTRIC SCOOTER, MODEL PIONEER 5 is the device name listed in this FDA 510(k) record. The listed applicant is Merits Health Products Co., Ltd.. It received FDA 510(k) clearance on 2001-12-11 under 510(k) number K013788. 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 TRAVEL EASE ELECTRIC SCOOTER, MODEL PIONEER 5?

TRAVEL EASE ELECTRIC SCOOTER, MODEL PIONEER 5 is a medical device that received FDA 510(k) clearance on 2001-12-11. The listed applicant is Merits Health Products Co., Ltd.. The 510(k) number is K013788.

When did TRAVEL EASE ELECTRIC SCOOTER, MODEL PIONEER 5 receive FDA 510(k) clearance?

TRAVEL EASE ELECTRIC SCOOTER, MODEL PIONEER 5 received FDA 510(k) clearance on 2001-12-11, under 510(k) number K013788.

Who is the listed applicant for TRAVEL EASE ELECTRIC SCOOTER, MODEL PIONEER 5?

The FDA 510(k) record lists Merits Health Products Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TRAVEL EASE ELECTRIC SCOOTER, MODEL PIONEER 5?

The FDA product code for TRAVEL EASE ELECTRIC SCOOTER, MODEL PIONEER 5 is 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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