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FDA 510(k)

ACTION-LIFT CHAIR

K-Number: K943330 · 1994-08-24

ApplicantAlc, Inc.
Decision Date1994-08-24
Product CodeINO
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

ACTION-LIFT CHAIR is the device name listed in this FDA 510(k) record. The listed applicant is Alc, Inc.. It received FDA 510(k) clearance on 1994-08-24 under 510(k) number K943330. 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 ACTION-LIFT CHAIR?

ACTION-LIFT CHAIR is a medical device that received FDA 510(k) clearance on 1994-08-24. The listed applicant is Alc, Inc.. The 510(k) number is K943330.

When did ACTION-LIFT CHAIR receive FDA 510(k) clearance?

ACTION-LIFT CHAIR received FDA 510(k) clearance on 1994-08-24, under 510(k) number K943330.

Who is the listed applicant for ACTION-LIFT CHAIR?

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

What is the FDA product code for ACTION-LIFT CHAIR?

The FDA product code for ACTION-LIFT CHAIR is INO.

Related Clinical Trials

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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.

K123834EASYSTAND BANTAM MEDIUMAltimate Medical, Inc.K112944FRESENIUS MEDICAL TREATMENT CHAIR T688 SERIESFresenius Medical Care South Asia Pacific Pty , Ltd.K101723COMPACT WHEELCHAIR PLATFORMDesign Specific FletcherK091578LIFT CHAIR, MODEL T3Pride Mobility Products Corp.K091727MEDICAL TREATMENT CHAIR, T400, T500,T600Fresenius Medical Care South Asia Pacific Pty , Ltd.K091242BANTAMAltimate Medical, Inc.

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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