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BIOPSY SCIENCES, LLC, LUNG BIOPSY SITE MARKER

K041331 Class II Traditional
Decision Date
2004-06-15
Sponsor / Applicant
Biopsy Sciences, LLC

Technical Specification

510(k) Submission ID K041331
Product Code GDW
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4750
Decision Date 2004-06-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BIOPSY SCIENCES, LLC, LUNG BIOPSY SITE MARKER received FDA 510(k) clearance under submission number K041331, sponsored by Biopsy Sciences, LLC. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 2004-06-15.

Classification & Regulation

This clearance is catalogued under FDA product code GDW and 21 CFR 878.4750, within the General, Plastic Surgery review panel as a Class II device.