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FDA 510(k)

TC SERIES (TILT RECLINER)

K-Number: K981419 · 1998-06-10

Decision Date1998-06-10
Product CodeIOR
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

TC SERIES (TILT RECLINER) is the device name listed in this FDA 510(k) record. The listed applicant is Get A Life-Give A Living Plus Kids Project, Inc.. It received FDA 510(k) clearance on 1998-06-10 under 510(k) number K981419. 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 TC SERIES (TILT RECLINER)?

TC SERIES (TILT RECLINER) is a medical device that received FDA 510(k) clearance on 1998-06-10. The listed applicant is Get A Life-Give A Living Plus Kids Project, Inc.. The 510(k) number is K981419.

When did TC SERIES (TILT RECLINER) receive FDA 510(k) clearance?

TC SERIES (TILT RECLINER) received FDA 510(k) clearance on 1998-06-10, under 510(k) number K981419.

Who is the listed applicant for TC SERIES (TILT RECLINER)?

The FDA 510(k) record lists Get A Life-Give A Living Plus Kids Project, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TC SERIES (TILT RECLINER)?

The FDA product code for TC SERIES (TILT RECLINER) 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 Get A Life-Give A Living Plus Kids Project, 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

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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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