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Nellcor EASYCAP II Adult Colorimetric CO2 Detector, Nellcor PEDCICAP Pediatric Colorimetric CO2 Detector

K203762 Class II Traditional
Decision Date
2021-09-17
Sponsor / Applicant
Covidien

Technical Specification

510(k) Submission ID K203762
Product Code CCK
Medical Specialty / Panel Anesthesiology
Regulation Citation 21 CFR 868.1400
Decision Date 2021-09-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Nellcor EASYCAP II Adult Colorimetric CO2 Detector, Nellcor PEDCICAP Pediatric Colorimetric CO2 Detector received FDA 510(k) clearance under submission number K203762, sponsored by Covidien. The device was reviewed via the Traditional premarket notification pathway and assigned to the Anesthesiology review panel. The statutory decision date of record is 2021-09-17.

Classification & Regulation

This clearance is catalogued under FDA product code CCK and 21 CFR 868.1400, within the Anesthesiology review panel as a Class II device.