GENESIS HEALTH TECHNOLOGIES BLOOD GLUCOSE MONITORING SYSTEM— 510(k) K121224
Substantially EquivalentTaidoc Technology Corporation
FDA 510(k) clearance K121224 for GENESIS HEALTH TECHNOLOGIES BLOOD GLUCOSE MONITORING SYSTEM, Substantially Equivalent on 2012-09-19. Applicant: Taidoc Technology Corporation. Device class: 2.
Clearance details
- Applicant
- Taidoc Technology Corporation
- Product code
- Code LFR
- Device class
- Class 2
- Regulation
- 21 CFR 862.1345
- Advisory panel
- Clinical Chemistry
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Location
- New Taipei City, TW
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More clearances from Taidoc Technology Corporation
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Adverse events under product code LFR
product code LFR- Death
- 3
- Malfunction
- 1,634
- Total
- 1,637
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.