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FDA 510(k)

STANDARD WHEELCHAIR PLATFORM

K-Number: K073565 · 2009-02-06

Decision Date2009-02-06
Product CodeINO
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

STANDARD WHEELCHAIR PLATFORM is the device name listed in this FDA 510(k) record. The listed applicant is Design Specific , Ltd.. It received FDA 510(k) clearance on 2009-02-06 under 510(k) number K073565. 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 STANDARD WHEELCHAIR PLATFORM?

STANDARD WHEELCHAIR PLATFORM is a medical device that received FDA 510(k) clearance on 2009-02-06. The listed applicant is Design Specific , Ltd.. The 510(k) number is K073565.

When did STANDARD WHEELCHAIR PLATFORM receive FDA 510(k) clearance?

STANDARD WHEELCHAIR PLATFORM received FDA 510(k) clearance on 2009-02-06, under 510(k) number K073565.

Who is the listed applicant for STANDARD WHEELCHAIR PLATFORM?

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

What is the FDA product code for STANDARD WHEELCHAIR PLATFORM?

The FDA product code for STANDARD WHEELCHAIR PLATFORM is INO.

Related Clinical Trials

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.

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.

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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