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FDA 510(k)

GOLDEN POWER LIFT CHAIR

K-Number: K880800 · 1988-03-14

Decision Date1988-03-14
Product CodeINO
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

GOLDEN POWER LIFT CHAIR is the device name listed in this FDA 510(k) record. The listed applicant is Golden Technologies, Inc.. It received FDA 510(k) clearance on 1988-03-14 under 510(k) number K880800. 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 GOLDEN POWER LIFT CHAIR?

GOLDEN POWER LIFT CHAIR is a medical device that received FDA 510(k) clearance on 1988-03-14. The listed applicant is Golden Technologies, Inc.. The 510(k) number is K880800.

When did GOLDEN POWER LIFT CHAIR receive FDA 510(k) clearance?

GOLDEN POWER LIFT CHAIR received FDA 510(k) clearance on 1988-03-14, under 510(k) number K880800.

Who is the listed applicant for GOLDEN POWER LIFT CHAIR?

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

What is the FDA product code for GOLDEN POWER LIFT CHAIR?

The FDA product code for GOLDEN POWER LIFT CHAIR is INO.

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 Golden Technologies, 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.

View all 8 devices →

Related Devices (Code: INO)

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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