FDA 510(k) FDA class 2 Substantially Equivalent 🇹🇼 Taiwan

HIVOX EAR THERMOMETER, TS SERIES

K Number: K020471 · Decision May 2, 2002
Classifications
1
FEI Numbers
488
Registration Numbers
488
Same Product Code
797
Applicant Total
18
Review Days
79

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
HIVOX EAR THERMOMETER, TS SERIES
K Number
K020471
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.2910
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Hivox Biotek, Inc.
Date Received
February 12, 2002
Decision Date
May 2, 2002
Product Code
FLL
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
FLL Continuous Measurement Thermometer

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (FLL), ordered by most recent decision date.

View all

Other Clearances by Hivox Biotek, Inc.

K Number Device Name
K260425 TENS / EMS DEVICE (FT-247 Series) (FT-247, FT-237)
K242815 POCKET TENS (EP-300)
K232675 Heating Tens, FT-615
K223308 HEATING TENS/EMS, FT-810R
K221384 Heating TENS/EMS Device, FT-240-1, Heating TENS/EMS Device, FT-240-2
K211403 HIVOX OTC Electrical Stimulator, FT610-B
K203574 HIVOX OTC Electrical Stimulator, EM59-l, HIVOX OTC Electrical Stimulator, EM59-2
K192264 HIVOX Spopad EMS SP-911, SP-921
K190347 HIVOX OTC Electrical Stimulator
K171803 HIVOX OTC Electrical Stimulator
Search all 18 clearances from Hivox Biotek, Inc. →