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FDA 510(k)

QUICKIE 2 POWER ASSIST WHEELCHAIR

K-Number: K001491 · 2000-12-15

Decision Date2000-12-15
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

QUICKIE 2 POWER ASSIST WHEELCHAIR is the device name listed in this FDA 510(k) record. The listed applicant is Sunrise Medical, Inc.. It received FDA 510(k) clearance on 2000-12-15 under 510(k) number K001491. 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 QUICKIE 2 POWER ASSIST WHEELCHAIR?

QUICKIE 2 POWER ASSIST WHEELCHAIR is a medical device that received FDA 510(k) clearance on 2000-12-15. The listed applicant is Sunrise Medical, Inc.. The 510(k) number is K001491.

When did QUICKIE 2 POWER ASSIST WHEELCHAIR receive FDA 510(k) clearance?

QUICKIE 2 POWER ASSIST WHEELCHAIR received FDA 510(k) clearance on 2000-12-15, under 510(k) number K001491.

Who is the listed applicant for QUICKIE 2 POWER ASSIST WHEELCHAIR?

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

What is the FDA product code for QUICKIE 2 POWER ASSIST WHEELCHAIR?

The FDA product code for QUICKIE 2 POWER ASSIST WHEELCHAIR is ITI.

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.

Other records listing Sunrise Medical, Inc. as applicant

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.

View all 19 devices →

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.

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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