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FDA 510(k)

BIOPSY SCIENCES, INC. HYDROMARK BREST BIOSY SITE MARKER

K-Number: K121113 · 2012-07-12

Decision Date2012-07-12
Product CodeNEU
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

BIOPSY SCIENCES, INC. HYDROMARK BREST BIOSY SITE MARKER is the device name listed in this FDA 510(k) record. The listed applicant is Biopsy Sciences, LLC. It received FDA 510(k) clearance on 2012-07-12 under 510(k) number K121113. 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 BIOPSY SCIENCES, INC. HYDROMARK BREST BIOSY SITE MARKER?

BIOPSY SCIENCES, INC. HYDROMARK BREST BIOSY SITE MARKER is a medical device that received FDA 510(k) clearance on 2012-07-12. The listed applicant is Biopsy Sciences, LLC. The 510(k) number is K121113.

When did BIOPSY SCIENCES, INC. HYDROMARK BREST BIOSY SITE MARKER receive FDA 510(k) clearance?

BIOPSY SCIENCES, INC. HYDROMARK BREST BIOSY SITE MARKER received FDA 510(k) clearance on 2012-07-12, under 510(k) number K121113.

Who is the listed applicant for BIOPSY SCIENCES, INC. HYDROMARK BREST BIOSY SITE MARKER?

The FDA 510(k) record lists Biopsy Sciences, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BIOPSY SCIENCES, INC. HYDROMARK BREST BIOSY SITE MARKER?

The FDA product code for BIOPSY SCIENCES, INC. HYDROMARK BREST BIOSY SITE MARKER is NEU.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Biopsy Sciences, LLC as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 8 devices →

Related Devices (Code: NEU)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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.

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