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FDA 510(k)

BUDDY WHEELCHAIR

K-Number: K960402 · 1996-02-16

ApplicantMetro-Care
Decision Date1996-02-16
Product CodeIOR
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

BUDDY WHEELCHAIR is the device name listed in this FDA 510(k) record. The listed applicant is Metro-Care. It received FDA 510(k) clearance on 1996-02-16 under 510(k) number K960402. 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 BUDDY WHEELCHAIR?

BUDDY WHEELCHAIR is a medical device that received FDA 510(k) clearance on 1996-02-16. The listed applicant is Metro-Care. The 510(k) number is K960402.

When did BUDDY WHEELCHAIR receive FDA 510(k) clearance?

BUDDY WHEELCHAIR received FDA 510(k) clearance on 1996-02-16, under 510(k) number K960402.

Who is the listed applicant for BUDDY WHEELCHAIR?

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

What is the FDA product code for BUDDY WHEELCHAIR?

The FDA product code for BUDDY 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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