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FDA 510(k)

TRX-CG CENTER-OF-GRAVITY SHIFTING POWER TILT AND RECLINE SYSTEMS

K-Number: K981837 · 1998-07-09

Decision Date1998-07-09
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

TRX-CG CENTER-OF-GRAVITY SHIFTING POWER TILT AND RECLINE SYSTEMS is the device name listed in this FDA 510(k) record. The listed applicant is Motion Concepts. It received FDA 510(k) clearance on 1998-07-09 under 510(k) number K981837. 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 CENTER-OF-GRAVITY SHIFTING POWER TILT AND RECLINE SYSTEMS?

TRX-CG CENTER-OF-GRAVITY SHIFTING POWER TILT AND RECLINE SYSTEMS is a medical device that received FDA 510(k) clearance on 1998-07-09. The listed applicant is Motion Concepts. The 510(k) number is K981837.

When did TRX-CG CENTER-OF-GRAVITY SHIFTING POWER TILT AND RECLINE SYSTEMS receive FDA 510(k) clearance?

TRX-CG CENTER-OF-GRAVITY SHIFTING POWER TILT AND RECLINE SYSTEMS received FDA 510(k) clearance on 1998-07-09, under 510(k) number K981837.

Who is the listed applicant for TRX-CG CENTER-OF-GRAVITY SHIFTING POWER TILT AND RECLINE SYSTEMS?

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 CENTER-OF-GRAVITY SHIFTING POWER TILT AND RECLINE SYSTEMS?

The FDA product code for TRX-CG CENTER-OF-GRAVITY SHIFTING POWER TILT AND RECLINE SYSTEMS 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

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

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