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DATASCOPE CA 40 8FR. IABS, MODEL 0684-00-04XX

K031569 Class II Special
Decision Date
2003-06-10
Sponsor / Applicant
Datascope Corp.

Technical Specification

510(k) Submission ID K031569
Product Code DSP
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.3535
Decision Date 2003-06-10
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DATASCOPE CA 40 8FR. IABS, MODEL 0684-00-04XX received FDA 510(k) clearance under submission number K031569, sponsored by Datascope Corp.. The device was reviewed via the Special premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2003-06-10.

Classification & Regulation

This clearance is catalogued under FDA product code DSP and 21 CFR 870.3535, within the Cardiovascular review panel as a Class II device.