FDA 510(k)

MANAN BIO-CUT SOFT TISSUE BIOPSY NEEDLE

K-Number: K052802 · 2005-11-01

Decision Date2005-11-01

Product CodeKNW

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

MANAN BIO-CUT SOFT TISSUE BIOPSY NEEDLE is the device name listed in this FDA 510(k) record. The listed applicant is Manan Medical Products, Inc.. It received FDA 510(k) clearance on 2005-11-01 under 510(k) number K052802. 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 BIO-CUT SOFT TISSUE BIOPSY NEEDLE?

MANAN BIO-CUT SOFT TISSUE BIOPSY NEEDLE is a medical device that received FDA 510(k) clearance on 2005-11-01. The listed applicant is Manan Medical Products, Inc.. The 510(k) number is K052802.

When did MANAN BIO-CUT SOFT TISSUE BIOPSY NEEDLE receive FDA 510(k) clearance?

MANAN BIO-CUT SOFT TISSUE BIOPSY NEEDLE received FDA 510(k) clearance on 2005-11-01, under 510(k) number K052802.

Who is the listed applicant for MANAN BIO-CUT SOFT TISSUE BIOPSY NEEDLE?

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

What is the FDA product code for MANAN BIO-CUT SOFT TISSUE BIOPSY NEEDLE?

The FDA product code for MANAN BIO-CUT SOFT TISSUE BIOPSY NEEDLE is 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.