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FDA 510(k)

KARE CHAIR I

K-Number: K900307 · 1990-02-15

ApplicantKare Chair Industries, Inc.
Decision Date1990-02-15
Product CodeINO
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

KARE CHAIR I is the device name listed in this FDA 510(k) record. The listed applicant is Kare Chair Industries, Inc.. It received FDA 510(k) clearance on 1990-02-15 under 510(k) number K900307. 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 KARE CHAIR I?

KARE CHAIR I is a medical device that received FDA 510(k) clearance on 1990-02-15. The listed applicant is Kare Chair Industries, Inc.. The 510(k) number is K900307.

When did KARE CHAIR I receive FDA 510(k) clearance?

KARE CHAIR I received FDA 510(k) clearance on 1990-02-15, under 510(k) number K900307.

Who is the listed applicant for KARE CHAIR I?

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

What is the FDA product code for KARE CHAIR I?

The FDA product code for KARE CHAIR I is INO.

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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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