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PCA-10, 10CC DISP. ANGIOGRAPHY CONTROL SYRINGE

K890292 Class II Traditional
Decision Date
1989-06-22
Sponsor / Applicant
Coeur Laboratories, Inc.

Technical Specification

510(k) Submission ID K890292
Product Code DXT
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1650
Decision Date 1989-06-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PCA-10, 10CC DISP. ANGIOGRAPHY CONTROL SYRINGE received FDA 510(k) clearance under submission number K890292, sponsored by Coeur Laboratories, 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 1989-06-22.

Classification & Regulation

This clearance is catalogued under FDA product code DXT and 21 CFR 870.1650, within the Cardiovascular review panel as a Class II device.