CMI 3000— 510(k) K854233
Substantially EquivalentCardio Management, Inc.
FDA 510(k) clearance K854233 for CMI 3000, Substantially Equivalent on 1986-01-08. Applicant: Cardio Management, Inc.. Device class: 2.
Clearance details
- Applicant
- Cardio Management, Inc.
- Product code
- Code DRO
- Device class
- Class 2
- Regulation
- 21 CFR 870.5550
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Birmingham, AL, US
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- K983232 — PADTAK PEDIATRIC DEFIB/CARDIOVERT/PACE/MONITOR-RADIOTRANSPARENT (2X2.25),MODEL 2602, PADTAK PEDIATRIC DEFIB/CARDIOVERT
Data sourced from openFDA. This site is unofficial and independent of the FDA.