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FDA 510(k)

HydroMARK Plus Breast Biopsy Site Marker

K-Number: K221961 · 2023-07-13

Decision Date2023-07-13
Product CodeNEU
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

HydroMARK Plus Breast Biopsy Site Marker is a medical device manufactured by Devicor Medical Products, Inc.. It received FDA 510(k) clearance on 2023-07-13 under approval number K221961. 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 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.

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Official Source

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