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RADIAL 4 HOT BIOPSY FORCEPS BOX 5; RADIAL JAW 4 HOT BIOPSY FORCEPS BOX 20; RADIAL JAW 4 HOT BIOPSY FORCEPS BOX 40

K101657 Class II Abbreviated
Decision Date
2010-10-05
Sponsor / Applicant
Boston Scientific Corp

Technical Specification

510(k) Submission ID K101657
Product Code KGE
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.4300
Decision Date 2010-10-05
Clearance Pathway Abbreviated

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

RADIAL 4 HOT BIOPSY FORCEPS BOX 5; RADIAL JAW 4 HOT BIOPSY FORCEPS BOX 20; RADIAL JAW 4 HOT BIOPSY FORCEPS BOX 40 received FDA 510(k) clearance under submission number K101657, sponsored by Boston Scientific Corp. The device was reviewed via the Abbreviated premarket notification pathway and assigned to the Gastroenterology, Urology review panel. The statutory decision date of record is 2010-10-05.

Classification & Regulation

This clearance is catalogued under FDA product code KGE and 21 CFR 876.4300, within the Gastroenterology, Urology review panel as a Class II device.