FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
Haemonetics Cell Saver Elite/Elite+ Autotransfusion System
K Number: K162423
·
Decision Jan 3, 2017
Classifications
1
FEI Numbers
54
Registration Numbers
54
Same Product Code
194
Applicant Total
1
Review Days
126
Basic Information
- Device Name
- Haemonetics Cell Saver Elite/Elite+ Autotransfusion System
- K Number
- K162423
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 868.5830
- Medical Specialty
- Anesthesiology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- HAEMONETICS CORPORATION
- Date Received
- August 30, 2016
- Decision Date
- January 3, 2017
- Product Code
- CAC
- Advisory Committee
- Anesthesiology
- Review Advisory Committee
- AN
- Third Party
- N
Classifications
This FDA 510(k) entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| CAC | Apparatus, Autotransfusion | FDA class 2 | Anesthesiology |
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