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FDA 510(k)

RENEGADE WHEELCHAIR

K-Number: K082857 · 2009-01-06

ApplicantAlpha One
Decision Date2009-01-06
Product CodeIQC
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

RENEGADE WHEELCHAIR is the device name listed in this FDA 510(k) record. The listed applicant is Alpha One. It received FDA 510(k) clearance on 2009-01-06 under 510(k) number K082857. The device is classified under product code IQC. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RENEGADE WHEELCHAIR?

RENEGADE WHEELCHAIR is a medical device that received FDA 510(k) clearance on 2009-01-06. The listed applicant is Alpha One. The 510(k) number is K082857.

When did RENEGADE WHEELCHAIR receive FDA 510(k) clearance?

RENEGADE WHEELCHAIR received FDA 510(k) clearance on 2009-01-06, under 510(k) number K082857.

Who is the listed applicant for RENEGADE WHEELCHAIR?

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

What is the FDA product code for RENEGADE WHEELCHAIR?

The FDA product code for RENEGADE WHEELCHAIR is IQC.

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Related Devices (Code: IQC)

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.

K251570Hippocampe Marathon and TrailVipamat SarlK120302MECHANICAL WHEELCHAIRNovaf Andalucia 2007, SLK051709HIPPOCAMPE WHEELCHAIRVipamat TechnologieK895384CALIFORNIA COMFORT FOUR WHEELJubilee Scooters, Inc.K861943PCI CUSTOM DESIGN SERIESPoston & Cole Intl.K843213QUALINE WHEELCHAIR PRODUCTSContemporary Health Sys

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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