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FDA 510(k)

TRX-CG POWER TILT AND RECLINE SYSTEM

K-Number: K990544 · 1999-04-08

Decision Date1999-04-08
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

TRX-CG POWER TILT AND RECLINE SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Motion Concepts. It received FDA 510(k) clearance on 1999-04-08 under 510(k) number K990544. The device is classified under product code ITI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRX-CG POWER TILT AND RECLINE SYSTEM?

TRX-CG POWER TILT AND RECLINE SYSTEM is a medical device that received FDA 510(k) clearance on 1999-04-08. The listed applicant is Motion Concepts. The 510(k) number is K990544.

When did TRX-CG POWER TILT AND RECLINE SYSTEM receive FDA 510(k) clearance?

TRX-CG POWER TILT AND RECLINE SYSTEM received FDA 510(k) clearance on 1999-04-08, under 510(k) number K990544.

Who is the listed applicant for TRX-CG POWER TILT AND RECLINE SYSTEM?

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

What is the FDA product code for TRX-CG POWER TILT AND RECLINE SYSTEM?

The FDA product code for TRX-CG POWER TILT AND RECLINE SYSTEM is ITI.

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 Motion Concepts 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 8 devices →

Related Devices (Code: ITI)

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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