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DATASCOPE PTCA PERCUTANEOUS CATHETER INTRODUCER

K901391 Class II Traditional
Decision Date
1990-06-26
Sponsor / Applicant
Datascope Corp.

Technical Specification

510(k) Submission ID K901391
Product Code DYB
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1340
Decision Date 1990-06-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DATASCOPE PTCA PERCUTANEOUS CATHETER INTRODUCER received FDA 510(k) clearance under submission number K901391, sponsored by Datascope 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 1990-06-26.

Classification & Regulation

This clearance is catalogued under FDA product code DYB and 21 CFR 870.1340, within the Cardiovascular review panel as a Class II device.