AMBULATORY ECG DIGITAL MONITOR MODEL: TD-30— 510(k) K880615
Substantially EquivalentCardiotechnics, Inc.
FDA 510(k) clearance K880615 for AMBULATORY ECG DIGITAL MONITOR MODEL: TD-30, Substantially Equivalent on 1988-05-13. Applicant: Cardiotechnics, Inc.. Device class: 2.
Clearance details
- Applicant
- Cardiotechnics, Inc.
- Product code
- Code DXH
- Device class
- Class 2
- Regulation
- 21 CFR 870.2920
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Big Spring, TX, US
Recent devices under product code DXH
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