FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
50MM WRITER MODEL CVM 9529
K Number: K792099
·
Decision Oct 26, 1979
Classifications
1
FEI Numbers
52
Registration Numbers
52
Same Product Code
86
Applicant Total
5
Review Days
7
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Basic Information
- Device Name
- 50MM WRITER MODEL CVM 9529
- K Number
- K792099
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 870.2810
- Medical Specialty
- Cardiovascular
- Decision
- Substantially Equivalent
- Applicant
- C-V Monitors Corp.
- Date Received
- October 19, 1979
- Decision Date
- October 26, 1979
- Product Code
- DSF
- Advisory Committee
- Cardiovascular
- Review Advisory Committee
- CV
- 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 |
|---|---|---|---|
| DSF | Recorder, Paper Chart | FDA class 1 | Cardiovascular |
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