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)

C350 POWERED WHEELCHAIR

K-Number: K071650 · 2007-09-12

ApplicantPermobil AB
Decision Date2007-09-12
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

C350 POWERED WHEELCHAIR is the device name listed in this FDA 510(k) record. The listed applicant is Permobil AB. It received FDA 510(k) clearance on 2007-09-12 under 510(k) number K071650. 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 C350 POWERED WHEELCHAIR?

C350 POWERED WHEELCHAIR is a medical device that received FDA 510(k) clearance on 2007-09-12. The listed applicant is Permobil AB. The 510(k) number is K071650.

When did C350 POWERED WHEELCHAIR receive FDA 510(k) clearance?

C350 POWERED WHEELCHAIR received FDA 510(k) clearance on 2007-09-12, under 510(k) number K071650.

Who is the listed applicant for C350 POWERED WHEELCHAIR?

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

What is the FDA product code for C350 POWERED WHEELCHAIR?

The FDA product code for C350 POWERED 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 Permobil AB 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.

K190682Explorer MiniK191874F5 Corpus VSK123290M300 & M400K103477PERMOBIL M300 / M400K081964K450 POWERED WHEELCHAIRK041219ELECTRO

View all 13 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.

↑