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)

SUPER CHAIR FOR KIDS BY ORION

K-Number: K103073 · 2011-01-03

Decision Date2011-01-03
Product CodeIOR
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

SUPER CHAIR FOR KIDS BY ORION is the device name listed in this FDA 510(k) record. The listed applicant is Future Mobility Healthcare, Inc.. It received FDA 510(k) clearance on 2011-01-03 under 510(k) number K103073. The device is classified under product code IOR. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SUPER CHAIR FOR KIDS BY ORION?

SUPER CHAIR FOR KIDS BY ORION is a medical device that received FDA 510(k) clearance on 2011-01-03. The listed applicant is Future Mobility Healthcare, Inc.. The 510(k) number is K103073.

When did SUPER CHAIR FOR KIDS BY ORION receive FDA 510(k) clearance?

SUPER CHAIR FOR KIDS BY ORION received FDA 510(k) clearance on 2011-01-03, under 510(k) number K103073.

Who is the listed applicant for SUPER CHAIR FOR KIDS BY ORION?

The FDA 510(k) record lists Future Mobility Healthcare, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SUPER CHAIR FOR KIDS BY ORION?

The FDA product code for SUPER CHAIR FOR KIDS BY ORION is IOR.

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 Future Mobility Healthcare, 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.

Related Devices (Code: IOR)

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.

↑