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FDA 510(k)

MOBILLIFE - MODEL (MOBIL RAIZER 22) - POWER WHEELCHAIR

K-Number: K061116 · 2006-07-03

ApplicantMobilife, LLC
Decision Date2006-07-03
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MOBILLIFE - MODEL (MOBIL RAIZER 22) - POWER WHEELCHAIR is the device name listed in this FDA 510(k) record. The listed applicant is Mobilife, LLC. It received FDA 510(k) clearance on 2006-07-03 under 510(k) number K061116. 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 MOBILLIFE - MODEL (MOBIL RAIZER 22) - POWER WHEELCHAIR?

MOBILLIFE - MODEL (MOBIL RAIZER 22) - POWER WHEELCHAIR is a medical device that received FDA 510(k) clearance on 2006-07-03. The listed applicant is Mobilife, LLC. The 510(k) number is K061116.

When did MOBILLIFE - MODEL (MOBIL RAIZER 22) - POWER WHEELCHAIR receive FDA 510(k) clearance?

MOBILLIFE - MODEL (MOBIL RAIZER 22) - POWER WHEELCHAIR received FDA 510(k) clearance on 2006-07-03, under 510(k) number K061116.

Who is the listed applicant for MOBILLIFE - MODEL (MOBIL RAIZER 22) - POWER WHEELCHAIR?

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

What is the FDA product code for MOBILLIFE - MODEL (MOBIL RAIZER 22) - POWER WHEELCHAIR?

The FDA product code for MOBILLIFE - MODEL (MOBIL RAIZER 22) - POWER WHEELCHAIR is ITI.

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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.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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