meddevicedb.com FDA Device Reference

PHARMASEAL OVER-THE NEEDLE ARTERIAL CATHETER & STA

K853714 Class II Traditional
Decision Date
1986-01-13
Sponsor / Applicant
American Pharmaseal Div. Ahsc

Technical Specification

510(k) Submission ID K853714
Product Code DQY
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1250
Decision Date 1986-01-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PHARMASEAL OVER-THE NEEDLE ARTERIAL CATHETER & STA received FDA 510(k) clearance under submission number K853714, sponsored by American Pharmaseal Div. Ahsc. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1986-01-13.

Classification & Regulation

This clearance is catalogued under FDA product code DQY and 21 CFR 870.1250, within the Cardiovascular review panel as a Class II device.