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FDA 510(k)

SERIES 9000 LIFT-RECLINE CHAIR

K-Number: K903905 · 1990-09-17

Decision Date1990-09-17
Product CodeINO
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

SERIES 9000 LIFT-RECLINE CHAIR is the device name listed in this FDA 510(k) record. The listed applicant is Equi-Tron Mfg., Inc.. It received FDA 510(k) clearance on 1990-09-17 under 510(k) number K903905. 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 SERIES 9000 LIFT-RECLINE CHAIR?

SERIES 9000 LIFT-RECLINE CHAIR is a medical device that received FDA 510(k) clearance on 1990-09-17. The listed applicant is Equi-Tron Mfg., Inc.. The 510(k) number is K903905.

When did SERIES 9000 LIFT-RECLINE CHAIR receive FDA 510(k) clearance?

SERIES 9000 LIFT-RECLINE CHAIR received FDA 510(k) clearance on 1990-09-17, under 510(k) number K903905.

Who is the listed applicant for SERIES 9000 LIFT-RECLINE CHAIR?

The FDA 510(k) record lists Equi-Tron Mfg., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SERIES 9000 LIFT-RECLINE CHAIR?

The FDA product code for SERIES 9000 LIFT-RECLINE 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 Equi-Tron Mfg., 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: 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

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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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