meddevicedb.com FDA Device Reference

PRIME CARE NEONATAL/PEDIATRIC TRACHEOSTOMY TUBE

K901920 Class II Traditional
Decision Date
1990-08-17
Sponsor / Applicant
Primecare, Inc.

Technical Specification

510(k) Submission ID K901920
Product Code BTO
Medical Specialty / Panel Anesthesiology
Regulation Citation 21 CFR 868.5800
Decision Date 1990-08-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PRIME CARE NEONATAL/PEDIATRIC TRACHEOSTOMY TUBE received FDA 510(k) clearance under submission number K901920, sponsored by Primecare, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Anesthesiology review panel. The statutory decision date of record is 1990-08-17.

Classification & Regulation

This clearance is catalogued under FDA product code BTO and 21 CFR 868.5800, within the Anesthesiology review panel as a Class II device.