FDA 510(k)

EASY LIFE

K-Number: K023521 · 2002-11-19

Decision Date2002-11-19

Product CodeINO

Advisory CommitteePM

DecisionSubstantially Equivalent

Device Summary

EASY LIFE is the device name listed in this FDA 510(k) record. The listed applicant is Berkline Corp.. It received FDA 510(k) clearance on 2002-11-19 under 510(k) number K023521. 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 EASY LIFE?

EASY LIFE is a medical device that received FDA 510(k) clearance on 2002-11-19. The listed applicant is Berkline Corp.. The 510(k) number is K023521.

When did EASY LIFE receive FDA 510(k) clearance?

EASY LIFE received FDA 510(k) clearance on 2002-11-19, under 510(k) number K023521.

Who is the listed applicant for EASY LIFE?

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

What is the FDA product code for EASY LIFE?

The FDA product code for EASY LIFE is INO.

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 Fletcher K091578LIFT CHAIR, MODEL T3Pride Mobility Products Corp.K091727MEDICAL TREATMENT CHAIR, T400, T500,T600Fresenius Medical Care South Asia Pacific Pty , Ltd.K091242BANTAMAltimate Medical, Inc.

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.