FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
STORAGE, DIGITAL DSC-1, CONTROL UNIT
K Number: K790288
·
Decision Feb 27, 1979
Classifications
1
FEI Numbers
63
Registration Numbers
63
Same Product Code
176
Applicant Total
48
Review Days
19
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Basic Information
- Device Name
- STORAGE, DIGITAL DSC-1, CONTROL UNIT
- K Number
- K790288
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 870.1435
- Medical Specialty
- Cardiovascular
- Decision
- Substantially Equivalent
- Applicant
- Oxford Medilog, Inc.
- Date Received
- February 8, 1979
- Decision Date
- February 27, 1979
- Product Code
- DXG
- 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 |
|---|---|---|---|
| DXG | Computer, Diagnostic, Pre-Programmed, Single-Function | FDA class 2 | Cardiovascular |
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| K902690 | SONICAID MODEL MERIDIAN 800 | Feb 5, 1991 | Substantially Equivalent |
| K895909 | SONICAID MODEL VASOFLO 4 | Jul 9, 1990 | Substantially Equivalent |
| K896535 | MEDILOG OPTIMA | Jan 18, 1990 | Substantially Equivalent |
| K891383 | MEDILOG 9200 EEG REPLAY/ANALYSIS SYSTEM | Jun 1, 1989 | Substantially Equivalent |
| K890330 | MEDILOG 6000-FD REPORT GENERATOR | Apr 20, 1989 | Substantially Equivalent |