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MAMMARY ASPIRATION SPECIMEN CYTOLOGY TEST

K030443 Class II Traditional
Decision Date
2003-05-09
Sponsor / Applicant
Nastech Pharmaceutical Company, Inc.

Technical Specification

510(k) Submission ID K030443
Product Code KNW
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.1075
Decision Date 2003-05-09
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MAMMARY ASPIRATION SPECIMEN CYTOLOGY TEST received FDA 510(k) clearance under submission number K030443, sponsored by Nastech Pharmaceutical Company, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Gastroenterology, Urology review panel. The statutory decision date of record is 2003-05-09.

Classification & Regulation

This clearance is catalogued under FDA product code KNW and 21 CFR 876.1075, within the Gastroenterology, Urology review panel as a Class II device.