FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
SIGNAL PROCESSOR/AVERAGER MODEL 7S11
K Number: K770878
·
Decision Jun 1, 1977
Classifications
1
FEI Numbers
57
Registration Numbers
57
Same Product Code
75
Applicant Total
8
Review Days
20
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Basic Information
- Device Name
- SIGNAL PROCESSOR/AVERAGER MODEL 7S11
- K Number
- K770878
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 882.1900
- Medical Specialty
- Neurology
- Decision
- Substantially Equivalent
- Applicant
- Medical Systems Corp.
- Date Received
- May 12, 1977
- Decision Date
- June 1, 1977
- Product Code
- GWJ
- Advisory Committee
- Neurology
- Review Advisory Committee
- NE
- 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 |
|---|---|---|---|
| GWJ | Stimulator, Auditory, Evoked Response | FDA class 2 | Neurology |
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