FDA 510(k)
FDA class 2
Substantially Equivalent
🇮🇹 Italy
CARDIOLINE AR 600, AR 1200, AR 2100
K Number: K051534
·
Decision Oct 5, 2005
Classifications
1
FEI Numbers
177
Registration Numbers
177
Same Product Code
574
Applicant Total
3
Review Days
117
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Basic Information
- Device Name
- CARDIOLINE AR 600, AR 1200, AR 2100
- K Number
- K051534
- Device Class
- FDA class 2
- Clearance Type
- Special
- Regulation Number
- 870.2340
- Medical Specialty
- Cardiovascular
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Et Medical Devices Spa
- Date Received
- June 10, 2005
- Decision Date
- October 5, 2005
- Product Code
- DPS
- 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 |
|---|---|---|---|
| DPS | Electrocardiograph | FDA class 2 | Cardiovascular |
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