FDA 510(k)

MANAN SOFT TISSUE BIOPSY NEEDLES

K-Number: K980122 · 1998-01-30

ApplicantMedical Device Technologies, Inc.

Decision Date1998-01-30

Product CodeKNW

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

MANAN SOFT TISSUE BIOPSY NEEDLES 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 1998-01-30 under 510(k) number K980122. 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 MANAN SOFT TISSUE BIOPSY NEEDLES?

MANAN SOFT TISSUE BIOPSY NEEDLES is a medical device that received FDA 510(k) clearance on 1998-01-30. The listed applicant is Medical Device Technologies, Inc.. The 510(k) number is K980122.

When did MANAN SOFT TISSUE BIOPSY NEEDLES receive FDA 510(k) clearance?

MANAN SOFT TISSUE BIOPSY NEEDLES received FDA 510(k) clearance on 1998-01-30, under 510(k) number K980122.

Who is the listed applicant for MANAN SOFT TISSUE BIOPSY NEEDLES?

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 MANAN SOFT TISSUE BIOPSY NEEDLES?

The FDA product code for MANAN SOFT TISSUE BIOPSY NEEDLES is KNW.

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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.