IEC CENTRA-7 CENTRIFUGE MODEL 2362— 510(k) K782124
Substantially EquivalentDamon Corp.
FDA 510(k) clearance K782124 for IEC CENTRA-7 CENTRIFUGE MODEL 2362, Substantially Equivalent on 1979-02-26. Applicant: Damon Corp.. Device class: 1.
Clearance details
- Applicant
- Damon Corp.
- Product code
- Code JQC
- Device class
- Class 1
- Regulation
- 21 CFR 862.2050
- Advisory panel
- Clinical Chemistry
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
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More clearances from Damon Corp.
view allAdverse events under product code JQC
product code JQC- Other
- 1
- Total
- 1
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.