510(k) K053000 ยท CAC Apparatus, Autotransfusion
HAEMONETICS CARDIOVASCULAR PERIOPERATIVE AUTOTRANSFUSION SYSTEM (CARDIOPAT)
| Applicant | Haemonetics Corp., Braintree MA, US |
| Decision | Substantially Equivalent, Nov 21, 2005 |
| Received | Oct 25, 2005 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K053000
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Aug 5, 2011 | Haemonetics Corporation Haemonetics cardioPAT -Cardiovascular Perioperative Autotransfusion System
Model 2050 US
Models Out-Side the US:
02050-UK, 02050-ES, 02050-IT, 02050-NL, 02050-GE, 02050-FR, 02050-JA
The Haemonetics C Terminated |
CAC | None listed |
| Feb 22, 2011 | Haemonetics Corporation Haemonetics cardioPAT Cardiovascular - autotransfusion System
Catalog Number: 02050-US Terminated |
CAC | None listed |
| Dec 8, 2007 | Haemonetics Corporation Haemonetics cardioPAT System, Product List Number 02050, Haemonetics Corporation, Braintree, MA 02184,(Cardiovascular Perioperative Autotransfusion) Terminated |
CAC | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.