DQH — Cardiograph, Apex (Vibrocardiograph) Class II
FDA product code DQH covers "Cardiograph, Apex (Vibrocardiograph)", a Class II medical device regulated under 21 CFR 870.2310. Submissions are reviewed by the Cardiovascular panel. At least 1 recent 510(k) clearance has been granted under this product code.
Classification Details
- Product Code
- DQH
- Device Class
- Class II
- Regulation Number
- 870.2310
- Submission Type
- Review Panel
- CV
- Medical Specialty
- Cardiovascular
- Implant
- No
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
|---|---|---|---|
| K974697 | bci intl | REUSABLE FINGER SENSOR 3444 | March 11, 1998 |