FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

FEVER TESTER

K Number: K790532 · Decision May 29, 1979
Classifications
1
FEI Numbers
40
Registration Numbers
40
Same Product Code
20
Applicant Total
51
Review Days
75

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Basic Information

Device Name
FEVER TESTER
K Number
K790532
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.2200
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Maddak, Inc.
Date Received
March 15, 1979
Decision Date
May 29, 1979
Product Code
KPD
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
KPD Strip, Temperature, Forehead, Liquid Crystal

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K841697 HYDRO-THERO PAD
K841692 PRONE STANDER
K841691 SPLIT SEAT POSITIONING CHAIR
K841693 STANDING FRAME
K834311 NIGHT TRAINER
K833870 KNEE WALKER
K833177 GLOSSECTOMY FEEDING SPOONS
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