FEVER TESTER— 510(k) K771980

Name: FDA 510(k) clearance K771980
Creator: U.S. Food and Drug Administration
Published: 1977-11-02

Substantially Equivalent

American Thermometer Company, Inc.

FDA 510(k) clearance K771980 for FEVER TESTER, Substantially Equivalent on 1977-11-02. Applicant: American Thermometer Company, Inc.. Device class: 2.

Clearance details

Applicant: American Thermometer Company, Inc.
Product code: Code KPD
Device class: Class 2
Regulation: 21 CFR 880.2200
Advisory panel: General Hospital
Date received: 1977-10-17
Decision date: 1977-11-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KPD

view all

K934941 — E-Z TEMP II1994-07-27
K903307 — TEMP MARQ TEMPERATURE TREND INDICATOR1990-08-17
K893803 — FEVER LINE AND FEVER LINE PLUS1989-08-21
K864853 — OMNI THERM TEMPERATURE MONITOR1987-02-04
K850797 — TEMPALERT LIQUID CRYSTAL THERMOMETER1985-04-05

More clearances from American Thermometer Company, Inc.

view all

K823245 — THERMAX; THERMAX SYSTEM1982-11-16
K821049 — PARATHERM1982-04-29

Data sourced from openFDA. This site is unofficial and independent of the FDA.