PACEPAC— 510(k) K852958
Substantially EquivalentMedical Data Electronics
FDA 510(k) clearance K852958 for PACEPAC, Substantially Equivalent on 1985-10-11. Applicant: Medical Data Electronics. Device class: 2.
Clearance details
- Applicant
- Medical Data Electronics
- 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
- Arleta, CA, US
Recent devices under product code DRO
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- K012404 — K-DEFIB/PACE ADULT ELECTRODE, MODEL KDP-85
- K000660 — ESCORT II+ 400 SERIES (ESCORT PRISM), MODEL 20400, 20401, 20403, MONITOR, MODELS 20411, 20412, 20413
- K983196 — PADTAK PACE/DEFIB/CARDIOVERT MONITORING ELECTRODE(S)
- K983232 — PADTAK PEDIATRIC DEFIB/CARDIOVERT/PACE/MONITOR-RADIOTRANSPARENT (2X2.25),MODEL 2602, PADTAK PEDIATRIC DEFIB/CARDIOVERT
More clearances from Medical Data Electronics
view all- K014294 — MODIFICATION TO ESCORT II+ 400 SERIES 9ESCORT PRISM) MONITOR, MODELS 20400, 20401, 20403, 20411, 20412, 20413, 20414
- K012336 — MODIFICATION TO:ESCORT VISION CENTRAL STATION TELEMETRY SYSTEM, MODEL 20500
- K992413 — ESCORT 100/300 SERIES B (ESCORT II) PATIENT MONITOR
- K992411 — ESCORT II+ 400 SERIES (ESCORT PRISM) MONITOR
- K982104 — ESCORT-LINK CENTRAL STATION MONITOR MODEL 20500
Data sourced from openFDA. This site is unofficial and independent of the FDA.