510(k) K222832

Device
Sentimag System
Applicant
Endomagnetics Ltd.,
510(k) number
K222832
Product code
NEU
Decision
Substantially Equivalent (SESE)
Decision date
2023-01-21
Date received
2022-09-20
Regulation
878.4300
Classification name
Marker, Radiographic, Implantable
Medical specialty
General, Plastic Surgery
Review panel
General, Plastic Surgery
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Applicant Contact#

Contact
Mehryar Behizad
Address
330 Cambridge Science Park, Milton Rd. Cambridge GB CB4 0WN CB4 0WN

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

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