MICROLIFE INSTANT DIGITAL ELECTRONIC THERMOMETER, MODEL MT19S1R— 510(k) K070590
Substantially EquivalentMicrolife Intellectual Property GmbH
FDA 510(k) clearance K070590 for MICROLIFE INSTANT DIGITAL ELECTRONIC THERMOMETER, MODEL MT19S1R, Substantially Equivalent on 2007-09-11. Applicant: Microlife Intellectual Property GmbH. Device class: 2.
Clearance details
- Applicant
- Microlife Intellectual Property GmbH
- Product code
- Code FLL
- Device class
- Class 2
- Regulation
- 21 CFR 880.2910
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Great Neck, NY, US
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- K211288 — Microlife Wrist Watch Blood Pressure Monitor Model BP3GK1-4B
Adverse events under product code FLL
product code FLL- Death
- 3
- Malfunction
- 557
- Total
- 560
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.