FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
COMMVIEW SYSTEM
K Number: K862715
·
Decision Oct 16, 1986
Classifications
1
FEI Numbers
159
Registration Numbers
159
Same Product Code
141
Applicant Total
1
Review Days
91
Basic Information
- Device Name
- COMMVIEW SYSTEM
- K Number
- K862715
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 892.2020
- Medical Specialty
- Radiology
- Decision
- Substantially Equivalent
- Applicant
- A T & T TECHNOLOGIES, INC.
- Date Received
- July 17, 1986
- Decision Date
- October 16, 1986
- Product Code
- LMD
- 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 |
|---|---|---|---|
| LMD | System, Digital Image Communications, Radiological | FDA class 1 | Radiology |
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