The following data is part of a premarket notification filed by Maquet Cardiopulmonary Ag with the FDA for Hlm Tubing Set With Bioline Coating.
| Device ID | K080592 |
| 510k Number | K080592 |
| Device Name: | HLM TUBING SET WITH BIOLINE COATING |
| Classification | Tubing, Pump, Cardiopulmonary Bypass |
| Applicant | MAQUET CARDIOPULMONARY AG HECHINGER STRASSE 38 Hirrlingen, DE 72145 |
| Contact | Katrin Schwenglenks |
| Correspondent | Katrin Schwenglenks MAQUET CARDIOPULMONARY AG HECHINGER STRASSE 38 Hirrlingen, DE 72145 |
| Product Code | DWE |
| Subsequent Product Code | DTL |
| Subsequent Product Code | DWF |
| CFR Regulation Number | 870.4390 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2008-03-03 |
| Decision Date | 2008-09-11 |
| Summary: | summary |