FDA 510(k)

V-CORE FULL CORE BREAST BIOPSY INSTRUMENT

K-Number: K042464 · 2004-09-30

ApplicantMedical Device Technologies, Inc.

Decision Date2004-09-30

Product CodeKNW

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

V-CORE FULL CORE BREAST BIOPSY INSTRUMENT 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 2004-09-30 under 510(k) number K042464. The device is classified under product code KNW. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the V-CORE FULL CORE BREAST BIOPSY INSTRUMENT?

V-CORE FULL CORE BREAST BIOPSY INSTRUMENT is a medical device that received FDA 510(k) clearance on 2004-09-30. The listed applicant is Medical Device Technologies, Inc.. The 510(k) number is K042464.

When did V-CORE FULL CORE BREAST BIOPSY INSTRUMENT receive FDA 510(k) clearance?

V-CORE FULL CORE BREAST BIOPSY INSTRUMENT received FDA 510(k) clearance on 2004-09-30, under 510(k) number K042464.

Who is the listed applicant for V-CORE FULL CORE BREAST BIOPSY INSTRUMENT?

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 V-CORE FULL CORE BREAST BIOPSY INSTRUMENT?

The FDA product code for V-CORE FULL CORE BREAST BIOPSY INSTRUMENT is KNW.

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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.