FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
ELI 150 ELECTROCARDIOGRAPH MODEL ELI 150
K Number: K101115
·
Decision Jun 18, 2010
Classifications
1
FEI Numbers
184
Registration Numbers
184
Same Product Code
570
Applicant Total
4
Review Days
58
Basic Information
- Device Name
- ELI 150 ELECTROCARDIOGRAPH MODEL ELI 150
- K Number
- K101115
- Device Class
- FDA class 2
- Clearance Type
- Abbreviated
- Regulation Number
- 870.2340
- Medical Specialty
- Cardiovascular
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- MORTARA INSTRUMENT, INC
- Date Received
- April 21, 2010
- Decision Date
- June 18, 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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