Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

TMC ELECTRICAL SCOOTER, EASY 405

K-Number: K031313 · 2003-09-04

Decision Date2003-09-04
Product CodeINI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

TMC ELECTRICAL SCOOTER, EASY 405 is the device name listed in this FDA 510(k) record. The listed applicant is Tmc Technology Corp.. It received FDA 510(k) clearance on 2003-09-04 under 510(k) number K031313. 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 TMC ELECTRICAL SCOOTER, EASY 405?

TMC ELECTRICAL SCOOTER, EASY 405 is a medical device that received FDA 510(k) clearance on 2003-09-04. The listed applicant is Tmc Technology Corp.. The 510(k) number is K031313.

When did TMC ELECTRICAL SCOOTER, EASY 405 receive FDA 510(k) clearance?

TMC ELECTRICAL SCOOTER, EASY 405 received FDA 510(k) clearance on 2003-09-04, under 510(k) number K031313.

Who is the listed applicant for TMC ELECTRICAL SCOOTER, EASY 405?

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

What is the FDA product code for TMC ELECTRICAL SCOOTER, EASY 405?

The FDA product code for TMC ELECTRICAL SCOOTER, EASY 405 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 Tmc Technology Corp. 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

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

↑