HydroMARK Plus Breast Biopsy Site Marker
K-Number: K221961 · 2023-07-13
Device Summary
Frequently Asked Questions
What is the HydroMARK Plus Breast Biopsy Site Marker?
HydroMARK Plus Breast Biopsy Site Marker is a medical device that received FDA 510(k) clearance on 2023-07-13. It is manufactured by Devicor Medical Products, Inc.. The 510(k) number is K221961.
When was HydroMARK Plus Breast Biopsy Site Marker approved by the FDA?
HydroMARK Plus Breast Biopsy Site Marker received FDA 510(k) clearance on 2023-07-13, under approval number K221961.
What company makes HydroMARK Plus Breast Biopsy Site Marker?
HydroMARK Plus Breast Biopsy Site Marker is manufactured by Devicor Medical Products, Inc..
What is the FDA product code for HydroMARK Plus Breast Biopsy Site Marker?
The FDA product code for HydroMARK Plus Breast Biopsy Site Marker is NEU.
Related Clinical Trials
Other Devices by Devicor Medical Products, Inc.
Related Devices (Code: NEU)
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.