FDA 510(k)

INTER V BRAND V-MARK BREAST BIOPSY SITE MARKER WITH TITANIUM ANCHOR

K-Number: K051421 · 2005-08-30

ApplicantMedical Device Technologies, Inc.

Decision Date2005-08-30

Product CodeNEU

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

INTER V BRAND V-MARK BREAST BIOPSY SITE MARKER WITH TITANIUM ANCHOR is the device name listed in this FDA 510(k) record. The listed applicant is Medical Device Technologies, Inc.. It received FDA 510(k) clearance on 2005-08-30 under 510(k) number K051421. 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 INTER V BRAND V-MARK BREAST BIOPSY SITE MARKER WITH TITANIUM ANCHOR?

INTER V BRAND V-MARK BREAST BIOPSY SITE MARKER WITH TITANIUM ANCHOR is a medical device that received FDA 510(k) clearance on 2005-08-30. The listed applicant is Medical Device Technologies, Inc.. The 510(k) number is K051421.

When did INTER V BRAND V-MARK BREAST BIOPSY SITE MARKER WITH TITANIUM ANCHOR receive FDA 510(k) clearance?

INTER V BRAND V-MARK BREAST BIOPSY SITE MARKER WITH TITANIUM ANCHOR received FDA 510(k) clearance on 2005-08-30, under 510(k) number K051421.

Who is the listed applicant for INTER V BRAND V-MARK BREAST BIOPSY SITE MARKER WITH TITANIUM ANCHOR?

The FDA 510(k) record lists Medical Device Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for INTER V BRAND V-MARK BREAST BIOPSY SITE MARKER WITH TITANIUM ANCHOR?

The FDA product code for INTER V BRAND V-MARK BREAST BIOPSY SITE MARKER WITH TITANIUM ANCHOR is NEU.

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Other records listing Medical Device Technologies, Inc. as applicant

K101832BIOPINCE ULTRA FULL CORE BIOPSY INSTRUMENT K053518INTERV BRAND V-MARK BREAST BIOPSY SITE MARKER WITH TITANIUM ANCHOR K050873CANALIZER HYDROPHILIC GUIDE WIRE K043523INTERV BRAND SNARELOK BONE MARROW BIOPSY NEEDLE K042464V-CORE FULL CORE BREAST BIOPSY INSTRUMENT K040427FIBREX CATHETER PATENCY DEVICE

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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.