FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
PHANTOM RADIOTRANSLUCENT ECG MONITORING ELECTRODE
K Number: K900682
·
Decision Jul 31, 1990
Classifications
1
FEI Numbers
21
Registration Numbers
21
Same Product Code
46
Applicant Total
4
Review Days
168
Basic Information
- Device Name
- PHANTOM RADIOTRANSLUCENT ECG MONITORING ELECTRODE
- K Number
- K900682
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 870.4330
- Medical Specialty
- Cardiovascular
- Decision
- Substantially Equivalent
- Applicant
- CONTOUR ELECTRODES, INC.
- Date Received
- February 13, 1990
- Decision Date
- July 31, 1990
- Product Code
- DRY
- 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 |
|---|---|---|---|
| DRY | Monitor, Blood-Gas, On-Line, Cardiopulmonary Bypass | FDA class 2 | Cardiovascular |
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