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FDA 510(k)

SUPREMA POWERED WHEELCHAIR

K-Number: K010600 · 2001-07-13

ApplicantLuigi Chinetti
Decision Date2001-07-13
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

SUPREMA POWERED WHEELCHAIR is the device name listed in this FDA 510(k) record. The listed applicant is Luigi Chinetti. It received FDA 510(k) clearance on 2001-07-13 under 510(k) number K010600. The device is classified under product code ITI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SUPREMA POWERED WHEELCHAIR?

SUPREMA POWERED WHEELCHAIR is a medical device that received FDA 510(k) clearance on 2001-07-13. The listed applicant is Luigi Chinetti. The 510(k) number is K010600.

When did SUPREMA POWERED WHEELCHAIR receive FDA 510(k) clearance?

SUPREMA POWERED WHEELCHAIR received FDA 510(k) clearance on 2001-07-13, under 510(k) number K010600.

Who is the listed applicant for SUPREMA POWERED WHEELCHAIR?

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

What is the FDA product code for SUPREMA POWERED WHEELCHAIR?

The FDA product code for SUPREMA POWERED WHEELCHAIR is ITI.

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Related Devices (Code: ITI)

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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