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MICROVASIVE LIPTHOTRIPSY PROBES

K973788 Class II Traditional
Decision Date
1998-01-21
Sponsor / Applicant
Boston Scientific Corp

Technical Specification

510(k) Submission ID K973788
Product Code FFK
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.4480
Decision Date 1998-01-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MICROVASIVE LIPTHOTRIPSY PROBES received FDA 510(k) clearance under submission number K973788, sponsored by Boston Scientific Corp. 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 1998-01-21.

Classification & Regulation

This clearance is catalogued under FDA product code FFK and 21 CFR 876.4480, within the Gastroenterology, Urology review panel as a Class II device.