F5 Corpus VS

Wheelchair, Standup

Permobil AB

The following data is part of a premarket notification filed by Permobil Ab with the FDA for F5 Corpus Vs.

Pre-market Notification Details

Device IDK191874
510k NumberK191874
Device Name:F5 Corpus VS
ClassificationWheelchair, Standup
Applicant Permobil AB Box 120 S-861 23 Timra,  SE
ContactIvan Fernandez
CorrespondentIvan Fernandez
Permobil AB Box 120 S-861 23 Timra,  SE
Product CodeIPL  
CFR Regulation Number890.3900 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received2019-07-12
Decision Date2019-10-25
Summary:summary

NIH GUDID Devices

Device IdentifiersubmissionNumberSupplement
17330818001006 K191874 000
17330818002003 K191874 000

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