← FDA Medical Device Classifications
Drug Eluting Permanent Left Ventricular (Lv) Pacemaker Electrode
OJX · Class III — High Risk (PMA approval required, life-sustaining) · Unknown
Classification
- FDA Product Code
OJX- 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
- Y
- Implant
- Y
- Third-party review
- N
Definition
Drug eluting permanent lv pacemaker electrodes are used with compatible cardiac rhythm therapy (crt) devices to deliver pacing pulses to the heart.
Market data
- Cleared 510(k) submissions
- 0
- Registered establishments
- 21
Source
- Authoritative
- FDA Device Classification database
- Machine
- JSON-LD · Markdown