PERMOBIL MINIOR

Wheelchair, Powered

PERMOBIL OF AMERICA

The following data is part of a premarket notification filed by Permobil Of America with the FDA for Permobil Minior.

Pre-market Notification Details

Device IDK870226
510k NumberK870226
Device Name:PERMOBIL MINIOR
ClassificationWheelchair, Powered
Applicant PERMOBIL OF AMERICA BOX 20 1644 MASSACHUSETTS AVENUE Lexington,  MA  02173
ContactFinkelstein, Md
CorrespondentFinkelstein, Md
PERMOBIL OF AMERICA BOX 20 1644 MASSACHUSETTS AVENUE Lexington,  MA  02173
Product CodeITI  
CFR Regulation Number890.3860 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1987-01-21
Decision Date1987-02-10

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.