MODEL 3110 HEART WIRE & 3110P PEDIATRIC HEART WIRE— 510(k) K890988
Substantially EquivalentPace Medical
FDA 510(k) clearance K890988 for MODEL 3110 HEART WIRE & 3110P PEDIATRIC HEART WIRE, Substantially Equivalent on 1989-08-25. Applicant: Pace Medical. Device class: 2.
Clearance details
- Applicant
- Pace Medical
- Product code
- Code LDF
- Device class
- Class 2
- Regulation
- 21 CFR 870.3680
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Waltham, MA, US
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More clearances from Pace Medical
view all- K011980 — ADAPTER, PACING ANALYZER/UNIVERSAL PACING ADAPTER, MODELS 4820 AND 4825
- K012392 — DISPOSABLE SURGICAL EXTENSION CABLE, MODEL 4255 AND MODEL 4260
- K002204 — PACEMAKER EXTENSION CABLE MODELS 4265,4265A, 4265V, 5265, 5265A, 5265V
- K002496 — MODEL 4815 ADAPTER
- K002497 — MODEL 4810 ANALYZER OUTPUT ADAPTER
Adverse events under product code LDF
product code LDF- Death
- 19
- Injury
- 188
- Malfunction
- 694
- Other
- 1
- Total
- 902
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Data sourced from openFDA. This site is unofficial and independent of the FDA.