FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
RECEPTAL ATS TRAUMA KGA1900L
K Number: K772196
·
Decision Dec 22, 1977
Classifications
1
FEI Numbers
54
Registration Numbers
54
Same Product Code
194
Applicant Total
69
Review Days
24
Basic Information
- Device Name
- RECEPTAL ATS TRAUMA KGA1900L
- K Number
- K772196
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 868.5830
- Medical Specialty
- Anesthesiology
- Decision
- Substantially Equivalent
- Applicant
- SORENSEN RESEARCH
- Date Received
- November 28, 1977
- Decision Date
- December 22, 1977
- Product Code
- CAC
- Advisory Committee
- Anesthesiology
- Review Advisory Committee
- HE
- 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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