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)

RED PACK MANLUAL POWER WHEELCHAIR CONVERSION KIT

K-Number: K940851 · 1995-02-03

ApplicantRedman, Inc.
Decision Date1995-02-03
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent for Some Indications

Device Summary

RED PACK MANLUAL POWER WHEELCHAIR CONVERSION KIT is the device name listed in this FDA 510(k) record. The listed applicant is Redman, Inc.. It received FDA 510(k) clearance on 1995-02-03 under 510(k) number K940851. The device is classified under product code ITI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the RED PACK MANLUAL POWER WHEELCHAIR CONVERSION KIT?

RED PACK MANLUAL POWER WHEELCHAIR CONVERSION KIT is a medical device that received FDA 510(k) clearance on 1995-02-03. The listed applicant is Redman, Inc.. The 510(k) number is K940851.

When did RED PACK MANLUAL POWER WHEELCHAIR CONVERSION KIT receive FDA 510(k) clearance?

RED PACK MANLUAL POWER WHEELCHAIR CONVERSION KIT received FDA 510(k) clearance on 1995-02-03, under 510(k) number K940851.

Who is the listed applicant for RED PACK MANLUAL POWER WHEELCHAIR CONVERSION KIT?

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

What is the FDA product code for RED PACK MANLUAL POWER WHEELCHAIR CONVERSION KIT?

The FDA product code for RED PACK MANLUAL POWER WHEELCHAIR CONVERSION KIT 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 Redman, 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.

K940852CHIEF STANDUP WHEELCHAIRK935751GERONIMO PRK940919CHIEF SRK940920ROAD SAVAGEK935750GERONIMOK935749ROAD WARRIOR

View all 16 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.

↑