THERMOMETER MODELS ST313C/F, ST314C/F, ST323C/F, ST324C/F, ST333C/F, ST334C/F— 510(k) K023956
Substantially EquivalentMesure Technology Co., Ltd.
FDA 510(k) clearance K023956 for THERMOMETER MODELS ST313C/F, ST314C/F, ST323C/F, ST324C/F, ST333C/F, ST334C/F, Substantially Equivalent on 2004-06-17. Applicant: Mesure Technology Co., Ltd.. Device class: 2.
Clearance details
- Applicant
- Mesure Technology Co., Ltd.
- 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
- San Chung City, TW
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More clearances from Mesure Technology Co., Ltd.
view all- K080981 — EAR THERMOMETER, MODELS ST66 AND ST67
- K071019 — DIGITAL CLINICAL THERMOMETER/MODELS ST8C SERIES
- K063542 — WIRELESS TEMPERATURE MONITOR / MODELS ST323C AND ST323F.
- K050303 — 5 SEC DIGITAL CLINICAL THERMOMETER, MODELS ST8630X, ST8640X, ST8730X, ST8740X, ST8930X, ST8940X, ST8030X, ST8040X.
- K042627 — EAR THERMOMETER MODELS ST61, ST62, ST63, ST64, AND ST65
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.