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LARGE TIP (4MM) DIAGNOSTIC-ELECTROHYSIOLOGY CATHETERS

K951744 Class II Traditional
Decision Date
1995-05-04
Sponsor / Applicant
Boston Scientific Corp

Technical Specification

510(k) Submission ID K951744
Product Code DRF
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1220
Decision Date 1995-05-04
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

LARGE TIP (4MM) DIAGNOSTIC-ELECTROHYSIOLOGY CATHETERS received FDA 510(k) clearance under submission number K951744, sponsored by Boston Scientific Corp. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1995-05-04.

Classification & Regulation

This clearance is catalogued under FDA product code DRF and 21 CFR 870.1220, within the Cardiovascular review panel as a Class II device.