FDA 510(k)
FDA class 2
Substantially Equivalent
🇩🇪 Germany
SENSOR MOBILE SM 100 VITAPHONE 1001R REMOS
K Number: K050670
·
Decision Mar 30, 2005
Classifications
1
FEI Numbers
80
Registration Numbers
80
Same Product Code
296
Applicant Total
2
Review Days
15
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Basic Information
- Device Name
- SENSOR MOBILE SM 100 VITAPHONE 1001R REMOS
- K Number
- K050670
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 870.2920
- Medical Specialty
- Cardiovascular
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Tms Telemedizinische Systeme GmbH
- Date Received
- March 15, 2005
- Decision Date
- March 30, 2005
- Product Code
- DXH
- Advisory Committee
- Cardiovascular
- Review Advisory Committee
- CV
- Third Party
- Y
Classifications
This FDA 510(k) entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| DXH | Transmitters And Receivers, Electrocardiograph, Telephone | FDA class 2 | Cardiovascular |
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Other Clearances by Tms Telemedizinische Systeme GmbH
| K Number | Device Name | ||
|---|---|---|---|
| K053378 | LOOP RECORDER VITAPHONE, 3100 SERIES | Feb 23, 2006 | Substantially Equivalent |