meddevicedb.com FDA Device Reference

LAGUNA SOFTIP DIAGNOSTIC CATHETERS

K961499 Class II Traditional
Decision Date
1996-10-17
Sponsor / Applicant
Boston Scientific Scimed, Inc.

Technical Specification

510(k) Submission ID K961499
Product Code DQO
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1200
Decision Date 1996-10-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

LAGUNA SOFTIP DIAGNOSTIC CATHETERS received FDA 510(k) clearance under submission number K961499, sponsored by Boston Scientific Scimed, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1996-10-17.

Classification & Regulation

This clearance is catalogued under FDA product code DQO and 21 CFR 870.1200, within the Cardiovascular review panel as a Class II device.