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FDA 510(k)

MINI POWER CHAIR, MODEL MN 5000

K-Number: K062483 · 2006-09-08

ApplicantLine Ind.(Shanghai) Co., Ltd.
Decision Date2006-09-08
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MINI POWER CHAIR, MODEL MN 5000 is the device name listed in this FDA 510(k) record. The listed applicant is Line Ind.(Shanghai) Co., Ltd.. It received FDA 510(k) clearance on 2006-09-08 under 510(k) number K062483. 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 MINI POWER CHAIR, MODEL MN 5000?

MINI POWER CHAIR, MODEL MN 5000 is a medical device that received FDA 510(k) clearance on 2006-09-08. The listed applicant is Line Ind.(Shanghai) Co., Ltd.. The 510(k) number is K062483.

When did MINI POWER CHAIR, MODEL MN 5000 receive FDA 510(k) clearance?

MINI POWER CHAIR, MODEL MN 5000 received FDA 510(k) clearance on 2006-09-08, under 510(k) number K062483.

Who is the listed applicant for MINI POWER CHAIR, MODEL MN 5000?

The FDA 510(k) record lists Line Ind.(Shanghai) Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MINI POWER CHAIR, MODEL MN 5000?

The FDA product code for MINI POWER CHAIR, MODEL MN 5000 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

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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