INFUSION PUMP PRIMER— 510(k) K834461
Substantially EquivalentParker Hannifin Corp.
FDA 510(k) clearance K834461 for INFUSION PUMP PRIMER, Substantially Equivalent on 1984-01-30. Applicant: Parker Hannifin Corp.. Device class: 2.
Clearance details
- Applicant
- Parker Hannifin Corp.
- Product code
- Code FRN
- Device class
- Class 2
- Regulation
- 21 CFR 880.5725
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Walker, MI, US
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More clearances from Parker Hannifin Corp.
view allAdverse events under product code FRN
product code FRN- Death
- 540
- Injury
- 6,178
- Malfunction
- 1,464,165
- Other
- 52
- Total
- 1,470,935
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.