HydroMARK Breast Biopsy Site Marker
K-Number: K161021 · 2016-05-05
Device Summary
Frequently Asked Questions
What is the HydroMARK Breast Biopsy Site Marker?
HydroMARK Breast Biopsy Site Marker is a medical device that received FDA 510(k) clearance on 2016-05-05. It is manufactured by Devicor Medical Products, Inc.. The 510(k) number is K161021.
When was HydroMARK Breast Biopsy Site Marker approved by the FDA?
HydroMARK Breast Biopsy Site Marker received FDA 510(k) clearance on 2016-05-05, under approval number K161021.
What company makes HydroMARK Breast Biopsy Site Marker?
HydroMARK Breast Biopsy Site Marker is manufactured by Devicor Medical Products, Inc..
What is the FDA product code for HydroMARK Breast Biopsy Site Marker?
The FDA product code for HydroMARK 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.