FDA 510(k)
FDA class 2
Substantially Equivalent
🇨🇳 China
PC ECG
K Number: K102854
·
Decision Dec 3, 2010
Classifications
1
FEI Numbers
184
Registration Numbers
184
Same Product Code
570
Applicant Total
47
Review Days
65
Basic Information
- Device Name
- PC ECG
- K Number
- K102854
- Device Class
- FDA class 2
- Clearance Type
- Special
- Regulation Number
- 870.2340
- Medical Specialty
- Cardiovascular
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- EDAN INSTRUMENTS, INC.
- Date Received
- September 29, 2010
- Decision Date
- December 3, 2010
- 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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