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FDA 510(k)

POWER SCOOTER, MODEL TL-688

K-Number: K042010 · 2004-09-01

Decision Date2004-09-01
Product CodeINI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

POWER SCOOTER, MODEL TL-688 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 2004-09-01 under 510(k) number K042010. 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 POWER SCOOTER, MODEL TL-688?

POWER SCOOTER, MODEL TL-688 is a medical device that received FDA 510(k) clearance on 2004-09-01. The listed applicant is Teh Lin Prosthetic & Orthopaedic, Inc.. The 510(k) number is K042010.

When did POWER SCOOTER, MODEL TL-688 receive FDA 510(k) clearance?

POWER SCOOTER, MODEL TL-688 received FDA 510(k) clearance on 2004-09-01, under 510(k) number K042010.

Who is the listed applicant for POWER SCOOTER, MODEL TL-688?

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 POWER SCOOTER, MODEL TL-688?

The FDA product code for POWER SCOOTER, MODEL TL-688 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 Teh Lin Prosthetic & Orthopaedic, Inc. 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.

View all 9 devices →

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

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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