FDA 510(k)

MEDICAL DEVICE TECHNOLOGIES MANUAL BIOPSY NEEDLE

K-Number: K944837 · 1994-10-14

ApplicantMedical Device Technologies, Inc.

Decision Date1994-10-14

Product CodeKNW

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

MEDICAL DEVICE TECHNOLOGIES MANUAL BIOPSY NEEDLE 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 1994-10-14 under 510(k) number K944837. 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 MEDICAL DEVICE TECHNOLOGIES MANUAL BIOPSY NEEDLE?

MEDICAL DEVICE TECHNOLOGIES MANUAL BIOPSY NEEDLE is a medical device that received FDA 510(k) clearance on 1994-10-14. The listed applicant is Medical Device Technologies, Inc.. The 510(k) number is K944837.

When did MEDICAL DEVICE TECHNOLOGIES MANUAL BIOPSY NEEDLE receive FDA 510(k) clearance?

MEDICAL DEVICE TECHNOLOGIES MANUAL BIOPSY NEEDLE received FDA 510(k) clearance on 1994-10-14, under 510(k) number K944837.

Who is the listed applicant for MEDICAL DEVICE TECHNOLOGIES MANUAL BIOPSY NEEDLE?

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 MEDICAL DEVICE TECHNOLOGIES MANUAL BIOPSY NEEDLE?

The FDA product code for MEDICAL DEVICE TECHNOLOGIES MANUAL BIOPSY NEEDLE is KNW.

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Other records listing Medical Device Technologies, Inc. as applicant

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Related Devices (Code: KNW)

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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.