Product code DQH— Cardiovascular
REUSABLE FINGER SENSOR 3444
- Classification name
- Cardiograph, Apex (Vibrocardiograph)
- Device class
- Class 2
- Regulation
- 21 CFR 870.2310
- Advisory panel
- Cardiovascular
- Total cleared
- 1
- First cleared
- Most recent
Market context for product code DQH
FDA has cleared device under product code DQH, all in 1998, filed by 1 applicant company. No FDA device recalls reference this product code. Class II devices are moderate-risk and subject to general and special controls; most reach market through 510(k) clearance by demonstrating substantial equivalence to a predicate device.
Top applicants under product code DQH
Recent clearances under product code DQH
Data sourced from openFDA. This site is unofficial and independent of the FDA.