FDA 510(k)

NASTECH MAMMARY ASPIRATION SPECIMAN CYTOLOGY TEST MASCT

K-Number: K012088 · 2001-12-18

ApplicantNastech Pharmaceutical Company, Inc.

Decision Date2001-12-18

Product CodeKNW

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

NASTECH MAMMARY ASPIRATION SPECIMAN CYTOLOGY TEST MASCT is the device name listed in this FDA 510(k) record. The listed applicant is Nastech Pharmaceutical Company, Inc.. It received FDA 510(k) clearance on 2001-12-18 under 510(k) number K012088. 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 NASTECH MAMMARY ASPIRATION SPECIMAN CYTOLOGY TEST MASCT?

NASTECH MAMMARY ASPIRATION SPECIMAN CYTOLOGY TEST MASCT is a medical device that received FDA 510(k) clearance on 2001-12-18. The listed applicant is Nastech Pharmaceutical Company, Inc.. The 510(k) number is K012088.

When did NASTECH MAMMARY ASPIRATION SPECIMAN CYTOLOGY TEST MASCT receive FDA 510(k) clearance?

NASTECH MAMMARY ASPIRATION SPECIMAN CYTOLOGY TEST MASCT received FDA 510(k) clearance on 2001-12-18, under 510(k) number K012088.

Who is the listed applicant for NASTECH MAMMARY ASPIRATION SPECIMAN CYTOLOGY TEST MASCT?

The FDA 510(k) record lists Nastech Pharmaceutical Company, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NASTECH MAMMARY ASPIRATION SPECIMAN CYTOLOGY TEST MASCT?

The FDA product code for NASTECH MAMMARY ASPIRATION SPECIMAN CYTOLOGY TEST MASCT is KNW.

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Official Source

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