The following data is part of a premarket notification filed by Maquet Cardiopulmonary Ag with the FDA for Venous Softbag Reservoirs With Softline Coating.
Device ID | K090690 |
510k Number | K090690 |
Device Name: | VENOUS SOFTBAG RESERVOIRS WITH SOFTLINE COATING |
Classification | Reservoir, Blood, Cardiopulmonary Bypass |
Applicant | MAQUET CARDIOPULMONARY AG HECHINGER STRASSE 38 Hirrlingen, DE 72145 |
Contact | Katrin Schwenkglenks |
Correspondent | Katrin Schwenkglenks MAQUET CARDIOPULMONARY AG HECHINGER STRASSE 38 Hirrlingen, DE 72145 |
Product Code | DTN |
CFR Regulation Number | 870.4400 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | Yes |
Date Received | 2009-03-16 |
Decision Date | 2009-12-23 |
Summary: | summary |
Device Identifier | submissionNumber | Supplement |
---|---|---|
04037691740331 | K090690 | 000 |