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FDA 510(k)

MECHANICAL DAILY USE WHEELCHAIR

K-Number: K021075 · 2002-07-12

ApplicantFirst World Services, Inc.
Decision Date2002-07-12
Product CodeIOR
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MECHANICAL DAILY USE WHEELCHAIR is the device name listed in this FDA 510(k) record. The listed applicant is First World Services, Inc.. It received FDA 510(k) clearance on 2002-07-12 under 510(k) number K021075. The device is classified under product code IOR. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MECHANICAL DAILY USE WHEELCHAIR?

MECHANICAL DAILY USE WHEELCHAIR is a medical device that received FDA 510(k) clearance on 2002-07-12. The listed applicant is First World Services, Inc.. The 510(k) number is K021075.

When did MECHANICAL DAILY USE WHEELCHAIR receive FDA 510(k) clearance?

MECHANICAL DAILY USE WHEELCHAIR received FDA 510(k) clearance on 2002-07-12, under 510(k) number K021075.

Who is the listed applicant for MECHANICAL DAILY USE WHEELCHAIR?

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

What is the FDA product code for MECHANICAL DAILY USE WHEELCHAIR?

The FDA product code for MECHANICAL DAILY USE WHEELCHAIR is IOR.

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Related Devices (Code: IOR)

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.

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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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