meddevicedb.com FDA Device Reference

NEONATAL INTRODUCER KIT

K820710 Class II Traditional
Decision Date
1982-04-01
Sponsor / Applicant
Norton Performance Plastics Corp.

Technical Specification

510(k) Submission ID K820710
Product Code DYB
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1340
Decision Date 1982-04-01
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

NEONATAL INTRODUCER KIT received FDA 510(k) clearance under submission number K820710, sponsored by Norton Performance Plastics 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 1982-04-01.

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.