FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
DATRIX CARDIO WIFI ELECTROCARDIOGRAPH
K Number: K053083
·
Decision Nov 30, 2005
Classifications
1
FEI Numbers
177
Registration Numbers
177
Same Product Code
574
Applicant Total
5
Review Days
28
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Basic Information
- Device Name
- DATRIX CARDIO WIFI ELECTROCARDIOGRAPH
- K Number
- K053083
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 870.2340
- Medical Specialty
- Cardiovascular
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Datrix
- Date Received
- November 2, 2005
- Decision Date
- November 30, 2005
- Product Code
- DPS
- 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 |
|---|---|---|---|
| DPS | Electrocardiograph | FDA class 2 | Cardiovascular |
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Other Clearances by Datrix
| K Number | Device Name | ||
|---|---|---|---|
| K052883 | CARDIOSERVER | Nov 1, 2005 | Substantially Equivalent |
| K031074 | DIGITAL AMBULATORY ECG (HOLTER) RECORDER | Oct 15, 2003 | Substantially Equivalent |
| K982975 | DIGITAL ECG HOLTER RECORDER, MODEL DR512 | Nov 10, 1998 | Substantially Equivalent |
| K921068 | GIKTER ECG CASSETTE TAPE RECORDER MODEL XR 300 | Mar 30, 1992 | Substantially Equivalent |