PLEXUS 2 & 3.5 HOLLOW FIBER OXYGENATORS
Device Facts
| Record ID | K931444 |
|---|---|
| Device Name | PLEXUS 2 & 3.5 HOLLOW FIBER OXYGENATORS |
| Applicant | Sorin Biomedica, Fiat, USA, Inc. |
| Product Code | DTZ · Cardiovascular |
| Decision Date | May 27, 1994 |
| Decision | SESE |
| Submission Type | Traditional |
| Regulation | 21 CFR 870.4350 |
| Device Class | Class 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.”
