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 |