COBE CML3

K880021 · Cobe Laboratories, Inc. · DTZ · Apr 1, 1988 · Cardiovascular

Device Facts

Record IDK880021
Device NameCOBE CML3
ApplicantCobe Laboratories, Inc.
Product CodeDTZ · Cardiovascular
Decision DateApr 1, 1988
DecisionSESE
Submission TypeTraditional
Regulation21 CFR 870.4350
Device ClassClass 2

Regulatory Classification

Identification

A cardiopulmonary bypass oxygenator is a device used to exchange gases between blood and a gaseous environment to satisfy the gas exchange needs of a patient during open-heart surgery.

Special Controls

*Classification.* Class II (special controls). The special control for this device is the FDA guidance document entitled “Guidance for Cardiopulmonary Bypass Oxygenators 510(k) Submissions.”

Innolitics
510(k) Summary
Decision Summary
Classification Order
Enter a record ID and click Load to view the document.
100%