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FDA 510(k)

INVACARE PLATINUM, MODELS IRC 5LX AND IRC 5LX02

K-Number: K020386 · 2002-07-02

ApplicantInvacare Corp.
Decision Date2002-07-02
Product CodeCAW
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

INVACARE PLATINUM, MODELS IRC 5LX AND IRC 5LX02 is the device name listed in this FDA 510(k) record. The listed applicant is Invacare Corp.. It received FDA 510(k) clearance on 2002-07-02 under 510(k) number K020386. The device is classified under product code CAW. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INVACARE PLATINUM, MODELS IRC 5LX AND IRC 5LX02?

INVACARE PLATINUM, MODELS IRC 5LX AND IRC 5LX02 is a medical device that received FDA 510(k) clearance on 2002-07-02. The listed applicant is Invacare Corp.. The 510(k) number is K020386.

When did INVACARE PLATINUM, MODELS IRC 5LX AND IRC 5LX02 receive FDA 510(k) clearance?

INVACARE PLATINUM, MODELS IRC 5LX AND IRC 5LX02 received FDA 510(k) clearance on 2002-07-02, under 510(k) number K020386.

Who is the listed applicant for INVACARE PLATINUM, MODELS IRC 5LX AND IRC 5LX02?

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

What is the FDA product code for INVACARE PLATINUM, MODELS IRC 5LX AND IRC 5LX02?

The FDA product code for INVACARE PLATINUM, MODELS IRC 5LX AND IRC 5LX02 is CAW.

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Other records listing Invacare Corp. as applicant

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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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