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FDA 510(k)

HIROLLER ELEVATING WHEELCHAIR

K-Number: K102837 · 2010-12-23

ApplicantMax Mobility, LLC
Decision Date2010-12-23
Product CodeIPL
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

HIROLLER ELEVATING WHEELCHAIR is the device name listed in this FDA 510(k) record. The listed applicant is Max Mobility, LLC. It received FDA 510(k) clearance on 2010-12-23 under 510(k) number K102837. The device is classified under product code IPL. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HIROLLER ELEVATING WHEELCHAIR?

HIROLLER ELEVATING WHEELCHAIR is a medical device that received FDA 510(k) clearance on 2010-12-23. The listed applicant is Max Mobility, LLC. The 510(k) number is K102837.

When did HIROLLER ELEVATING WHEELCHAIR receive FDA 510(k) clearance?

HIROLLER ELEVATING WHEELCHAIR received FDA 510(k) clearance on 2010-12-23, under 510(k) number K102837.

Who is the listed applicant for HIROLLER ELEVATING WHEELCHAIR?

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

What is the FDA product code for HIROLLER ELEVATING WHEELCHAIR?

The FDA product code for HIROLLER ELEVATING WHEELCHAIR is IPL.

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Other records listing Max Mobility, LLC 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.

K113621SMARTDRIVE WHEELCHAIR POWER-ASSIST

Related Devices (Code: IPL)

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.

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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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