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FDA 510(k)

MOBILCHAIR 360 ELECTRIC-POWERED CHAIR

K-Number: K844847 · 1985-03-13

ApplicantDavis-Smith Corp.
Decision Date1985-03-13
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MOBILCHAIR 360 ELECTRIC-POWERED CHAIR is the device name listed in this FDA 510(k) record. The listed applicant is Davis-Smith Corp.. It received FDA 510(k) clearance on 1985-03-13 under 510(k) number K844847. 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 MOBILCHAIR 360 ELECTRIC-POWERED CHAIR?

MOBILCHAIR 360 ELECTRIC-POWERED CHAIR is a medical device that received FDA 510(k) clearance on 1985-03-13. The listed applicant is Davis-Smith Corp.. The 510(k) number is K844847.

When did MOBILCHAIR 360 ELECTRIC-POWERED CHAIR receive FDA 510(k) clearance?

MOBILCHAIR 360 ELECTRIC-POWERED CHAIR received FDA 510(k) clearance on 1985-03-13, under 510(k) number K844847.

Who is the listed applicant for MOBILCHAIR 360 ELECTRIC-POWERED CHAIR?

The FDA 510(k) record lists Davis-Smith Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MOBILCHAIR 360 ELECTRIC-POWERED CHAIR?

The FDA product code for MOBILCHAIR 360 ELECTRIC-POWERED CHAIR 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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