Atlas FDA

FEVER TESTER

FDA 510(k) clearance K790532 · decided 1979-05-29

Clearance details

K-number
K790532
Device name
FEVER TESTER
Applicant
Maddak, Inc.
Decision
Substantially Equivalent
Date received
1979-03-15
Decision date
1979-05-29
Days to decision
75 days
Clearance type
Traditional
Product code
KPD
Device class
2
Regulation number
880.2200
Medical specialty
General Hospital
Advisory committee
General Hospital
Location
Mchenry, IL, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
E-Z TEMP II (K934941)Seven C'S, Inc.1994-07-27
TEMP MARQ TEMPERATURE TREND INDICATOR (K903307)Marquest Medical Products, Inc.1990-08-17
FEVER LINE AND FEVER LINE PLUS (K893803)Liquid Crystal Sciences, Inc.1989-08-21
OMNI THERM TEMPERATURE MONITOR (K864853)Omni Therm, Inc.1987-02-04
TEMPALERT LIQUID CRYSTAL THERMOMETER (K850797)Medical Frontiers, Inc.1985-04-05
TEMPTREND PEDS AXILLARY TEMP. INDICATOR (K841913)Biosynergy, Inc.1984-11-02
TEMPTREND II (K833904)Biosynergy, Inc.1983-12-27
ATI FOREHEAD THERMOMETER (K832651)American Thermal Instruments, Inc.1983-10-04
ACCA-TEMP SKIN TEMP. VINYL DISC (K823221)T. G. & E. Medical1983-01-12
TEMPTREND TEMPERATURE TREND INDICATOR (K821312)Liquid Crystal Products, Inc.1982-05-28
TEMPERATURE TREND INDICATOR (TTI) (K820426)Mon-A-Therm, Inc.1982-03-08
SKIN TEMPERATURE SENSING VINYL STRIP (K813199)T. G. & E. Medical1982-03-05

Recalls involving this device

No recalls on record reference this clearance.