Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

QUICKIE RHAPSODY, MWD SERIES II POWER WHEELCHAIR

K-Number: K062701 · 2006-09-25

ApplicantSunrise Medical, Inc.
Decision Date2006-09-25
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

QUICKIE RHAPSODY, MWD SERIES II POWER 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 2006-09-25 under 510(k) number K062701. 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 RHAPSODY, MWD SERIES II POWER WHEELCHAIR?

QUICKIE RHAPSODY, MWD SERIES II POWER WHEELCHAIR is a medical device that received FDA 510(k) clearance on 2006-09-25. The listed applicant is Sunrise Medical, Inc.. The 510(k) number is K062701.

When did QUICKIE RHAPSODY, MWD SERIES II POWER WHEELCHAIR receive FDA 510(k) clearance?

QUICKIE RHAPSODY, MWD SERIES II POWER WHEELCHAIR received FDA 510(k) clearance on 2006-09-25, under 510(k) number K062701.

Who is the listed applicant for QUICKIE RHAPSODY, MWD SERIES II POWER 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 RHAPSODY, MWD SERIES II POWER WHEELCHAIR?

The FDA product code for QUICKIE RHAPSODY, MWD SERIES II POWER 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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

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.

K072153QUICKIE QX MANUAL FOLDING WHEELCHAIRK031289QUICKIE FREESTYLE POWER WHEELCHAIR, MODEL G-424K010917POWER TILT AND RECLINE SYSTEMK011268BREEZY WHEELCHAIR, MODEL 300K001491QUICKIE 2 POWER ASSIST WHEELCHAIRK981885SUNRISE SCOOTER SERIES, MODEL UNASSIGNED, 3 WHEEL STANDARD MODEL, 3 WHEEL MID RANGE MODEL, 3 WHEEL HIGH END MODEL, 4 WHE

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.

K262582Electric wheelchair (GP100)Suzhou Green Pine Medical Co., Ltd.K262054Electric WheelchairYongkang Joymax Medical Technology Co., Ltd.K260053Power Wheelchair (OS-R-M01I)Beijing OrionStar Technology Co., Ltd.K260229Electric wheelchair (HC819N, HC830N, HC831N)Yongkang Hengyi Vehicle Co., Ltd.K261354Electric wheelchair (D03)Foshan Sowell Medical Technology Co., Ltd.K261149Electric Wheelchair (DY611A-2, DY612A-1)Zhejiang Lumbre Electric Appliance Co., Ltd.

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.

↑