FDA 510(k) FDA class 2 Substantially Equivalent 🇦🇹 Austria

SteadyTemp

K Number: K233280 · Decision Jun 21, 2024
Classifications
1
FEI Numbers
488
Registration Numbers
488
Same Product Code
797
Applicant Total
1
Review Days
266

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Basic Information

Device Name
SteadyTemp
K Number
K233280
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.2910
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Steadysense GmbH
Date Received
September 29, 2023
Decision Date
June 21, 2024
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

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