The following data is part of a premarket notification filed by Maquet Cardiopulmonary Ag with the FDA for Hlm Tubing Set With Softline Coating.
| Device ID | K090533 |
| 510k Number | K090533 |
| Device Name: | HLM TUBING SET WITH SOFTLINE COATING |
| Classification | Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass |
| Applicant | MAQUET CARDIOPULMONARY AG HECHINGER STRASSE 38 Hirrlingen, DE 72145 |
| Contact | Ingrid Richter |
| Correspondent | Ingrid Richter MAQUET CARDIOPULMONARY AG HECHINGER STRASSE 38 Hirrlingen, DE 72145 |
| Product Code | DWF |
| CFR Regulation Number | 870.4210 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | Yes |
| Date Received | 2009-02-27 |
| Decision Date | 2009-12-18 |
| Summary: | summary |