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FDA 510(k)

SCOOTER MARS SERIES, MODEL TL-588

K-Number: K022698 · 2002-12-02

ApplicantTeh Lin Prosthetic & Orthopaedic, Inc.
Decision Date2002-12-02
Product CodeINI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

SCOOTER MARS SERIES, MODEL TL-588 is the device name listed in this FDA 510(k) record. The listed applicant is Teh Lin Prosthetic & Orthopaedic, Inc.. It received FDA 510(k) clearance on 2002-12-02 under 510(k) number K022698. 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 SCOOTER MARS SERIES, MODEL TL-588?

SCOOTER MARS SERIES, MODEL TL-588 is a medical device that received FDA 510(k) clearance on 2002-12-02. The listed applicant is Teh Lin Prosthetic & Orthopaedic, Inc.. The 510(k) number is K022698.

When did SCOOTER MARS SERIES, MODEL TL-588 receive FDA 510(k) clearance?

SCOOTER MARS SERIES, MODEL TL-588 received FDA 510(k) clearance on 2002-12-02, under 510(k) number K022698.

Who is the listed applicant for SCOOTER MARS SERIES, MODEL TL-588?

The FDA 510(k) record lists Teh Lin Prosthetic & Orthopaedic, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SCOOTER MARS SERIES, MODEL TL-588?

The FDA product code for SCOOTER MARS SERIES, MODEL TL-588 is INI.

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Other records listing Teh Lin Prosthetic & Orthopaedic, Inc. 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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