510(k) K221841

Device
EOlife®
Applicant
Archeon
510(k) number
K221841
Product code
BTM
Decision
Substantially Equivalent (SESE)
Decision date
2023-03-18
Date received
2022-06-24
Regulation
868.5915
Classification name
Ventilator, Emergency, Manual (Resuscitator)
Medical specialty
Anesthesiology
Review panel
Anesthesiology
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Applicant Contact#

Contact
Valentine OQDA
Address
2 Chemin Des Aiguillettes Besançon FR 25000 25000

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

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510(k), Device, Applicant table
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K094003REVIVATORHersill, S.L.2010-09-17
K093081POCKET BVMMicrobvm Systems , Ltd.2010-02-05
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