FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
TELEVISION CONTROL OPTION 1220
K Number: K850314
·
Decision Apr 25, 1985
Classifications
1
FEI Numbers
17
Registration Numbers
17
Same Product Code
23
Applicant Total
4
Review Days
90
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Basic Information
- Device Name
- TELEVISION CONTROL OPTION 1220
- K Number
- K850314
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 890.3725
- Medical Specialty
- Physical Medicine
- Decision
- Substantially Equivalent
- Applicant
- Rehab Technology, Inc.
- Date Received
- January 25, 1985
- Decision Date
- April 25, 1985
- Product Code
- IQA
- Advisory Committee
- Physical Medicine
- Review Advisory Committee
- PM
- 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 |
|---|---|---|---|
| IQA | System, Environmental Control, Powered | FDA class 2 | Physical Medicine |
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