meddevicedb.com FDA Device Reference

MODIFICATION TO: SIPAP INFANT NASAL CPAP CIRCUIT

K012034 Class II Special
Decision Date
2001-07-24
Sponsor / Applicant
Sensor Medics Corp.

Technical Specification

510(k) Submission ID K012034
Product Code BZD
Medical Specialty / Panel Anesthesiology
Regulation Citation 21 CFR 868.5905
Decision Date 2001-07-24
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MODIFICATION TO: SIPAP INFANT NASAL CPAP CIRCUIT received FDA 510(k) clearance under submission number K012034, sponsored by Sensor Medics Corp.. The device was reviewed via the Special premarket notification pathway and assigned to the Anesthesiology review panel. The statutory decision date of record is 2001-07-24.

Classification & Regulation

This clearance is catalogued under FDA product code BZD and 21 CFR 868.5905, within the Anesthesiology review panel as a Class II device.