FDA 510(k)

LIFT CHAIR, MODEL T3

K-Number: K091578 · 2009-12-02

Decision Date2009-12-02

Product CodeINO

Advisory CommitteePM

DecisionSubstantially Equivalent

Device Summary

LIFT CHAIR, MODEL T3 is the device name listed in this FDA 510(k) record. The listed applicant is Pride Mobility Products Corp.. It received FDA 510(k) clearance on 2009-12-02 under 510(k) number K091578. The device is classified under product code INO. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIFT CHAIR, MODEL T3?

LIFT CHAIR, MODEL T3 is a medical device that received FDA 510(k) clearance on 2009-12-02. The listed applicant is Pride Mobility Products Corp.. The 510(k) number is K091578.

When did LIFT CHAIR, MODEL T3 receive FDA 510(k) clearance?

LIFT CHAIR, MODEL T3 received FDA 510(k) clearance on 2009-12-02, under 510(k) number K091578.

Who is the listed applicant for LIFT CHAIR, MODEL T3?

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

What is the FDA product code for LIFT CHAIR, MODEL T3?

The FDA product code for LIFT CHAIR, MODEL T3 is INO.

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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.