inforMED
IMRClass I

Device, Anti-tip, Wheelchair

Physical Medicine · 21 CFR 890.3920

MDR events6All time
Recalls0All time
Registered firms56Currently listed
510(k) clearances0All time

Recent MDR events

6 adverse event reports on file

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Event type breakdown

Malfunction5
Other1

Most-reported manufacturers

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Tisport, Llc5Innovative Products Unlimited1

Recalls

0 recall events for this product code

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No recalls on file for this product code.

Registered firms

56 firms currently registered for this product code

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510(k) clearances

0 clearances for this product code

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No 510(k) clearances on file for this product code.