510(k) K251989

Device
VizMark Preloaded Tissue Marker Device (VM-0001)
Applicant
Breast-Med, Inc.
510(k) number
K251989
Product code
NEU
Decision
Substantially Equivalent (SESE)
Decision date
2025-12-12
Date received
2025-06-27
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
N
Source
FDA openFDA 510(k) dataset plus migrated FDA.report data

Related Records

Applicant Contact

Contact
Michael Nelson
Address
10580 Wayzata Blvd. Suite 150 Hopkins MN US 55305 55305

FDA Registration Numbers

Source Documents

FDA 510(k) Premarket Notification Database · 510(k) summary PDF · openFDA JSON

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