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FDA 510(k)

HydroMARK Breast Biopsy Site Marker

K-Number: K161021 · 2016-05-05

Decision Date2016-05-05
Product CodeNEU
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

HydroMARK Breast Biopsy Site Marker is a medical device manufactured by Devicor Medical Products, Inc.. It received FDA 510(k) clearance on 2016-05-05 under approval number K161021. The device is classified under product code NEU. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

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.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.