FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
TARGET CAT#B7850AA & B7850AB & B7850B
K Number: K851301
·
Decision Sep 20, 1985
Classifications
1
FEI Numbers
27
Registration Numbers
27
Same Product Code
91
Applicant Total
254
Review Days
172
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Basic Information
- Device Name
- TARGET CAT#B7850AA & B7850AB & B7850B
- K Number
- K851301
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 892.5050
- Medical Specialty
- Radiology
- Decision
- Substantially Equivalent
- Applicant
- General Electric Co.
- Date Received
- April 1, 1985
- Decision Date
- September 20, 1985
- Product Code
- LHN
- Advisory Committee
- Radiology
- Review Advisory Committee
- RA
- 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 |
|---|---|---|---|
| LHN | System, Radiation Therapy, Charged-Particle, Medical | FDA class 2 | Radiology |
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