Product code KPD— General Hospital
FEVER TESTER
- Classification name
- Strip, Temperature, Forehead, Liquid Crystal
- Device class
- Class 2
- Regulation
- 21 CFR 880.2200
- Advisory panel
- General Hospital
- Total cleared
- 21
- First cleared
- Most recent
Market context for product code KPD
FDA has cleared devices under product code KPD between 1976 and 1994, filed by 18 applicant companies. No FDA device recalls reference this product code. Class II devices are moderate-risk and subject to general and special controls; most reach market through 510(k) clearance by demonstrating substantial equivalence to a predicate device.
Clearances per year
- 1994
- 1990
- 1989
- 1987
- 1985
- 1984
- 1983
- 1982
- 1981
- 1980
- 1979
- 1978
- 1977
- 1976
Top applicants under product code KPD
Recent clearances under product code KPD
- K934941 — E-Z TEMP II
- K903307 — TEMP MARQ TEMPERATURE TREND INDICATOR
- K893803 — FEVER LINE AND FEVER LINE PLUS
- K864853 — OMNI THERM TEMPERATURE MONITOR
- K850797 — TEMPALERT LIQUID CRYSTAL THERMOMETER
- K841913 — TEMPTREND PEDS AXILLARY TEMP. INDICATOR
- K833904 — TEMPTREND II
- K832651 — ATI FOREHEAD THERMOMETER
- K823221 — ACCA-TEMP SKIN TEMP. VINYL DISC
- K821312 — TEMPTREND TEMPERATURE TREND INDICATOR
- K820426 — TEMPERATURE TREND INDICATOR (TTI)
- K813199 — SKIN TEMPERATURE SENSING VINYL STRIP
- K802778 — LIQUID CRYSTAL THERM. 8 EVENT MONITOR
- K802897 — ELECTRONIC DIGITAL THERMOMETER
- K790532 — FEVER TESTER
- K780580 — TEMPERATURE INDICATOR
- K780260 — TEMP. SENSOR W/22MM FITTINGS
- K771980 — FEVER TESTER
- K770517 — NF DEVICE
- K770353 — DISPOSABLE TEMPERATURE PROBE
- K760683 — ALARM, THERMAL, THERM-ALERT
Data sourced from openFDA. This site is unofficial and independent of the FDA.