← FDA Medical Device Classifications
Acute Coronary Syndrome Event Detector
QBI · Class III — High Risk (PMA approval required, life-sustaining) · Unknown
Classification
- FDA Product Code
QBI- Device class
- Class III — High Risk (PMA approval required, life-sustaining)
- Regulation
- —
- Review panel
- CV
- Medical specialty
- Unknown
- Submission type
- 2
- GMP exempt
- N
- Life sustaining
- N
- Implant
- Y
- Third-party review
- N
Definition
Detect Acute Coronary Syndrome events and prompt the patient to seek medical attention.
Market data
- Cleared 510(k) submissions
- 0
- Registered establishments
- 3
Source
- Authoritative
- FDA Device Classification database
- Machine
- JSON-LD · Markdown