FDA 510(k) FDA class 2 Substantially Equivalent 🇯🇵 Japan

TOSHIBA DIGITAL CLINICAL THERMOMTER

K Number: K852903 · Decision Jul 24, 1985
Classifications
1
FEI Numbers
488
Registration Numbers
488
Same Product Code
797
Applicant Total
54
Review Days
15

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Basic Information

Device Name
TOSHIBA DIGITAL CLINICAL THERMOMTER
K Number
K852903
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.2910
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Toshiba Medical Systems
Date Received
July 9, 1985
Decision Date
July 24, 1985
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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Other Clearances by Toshiba Medical Systems

K Number Device Name
K960948 SCATTER CORRECTION VOLUME SOFTWARE MODEL NSSC-020A
K954310 BLA-800A
K954309 ANGIOREX
K893750 MRT-50A MOBILE
K891453 DIAGNOSTIC ULTRASOUND TRANSDUCER: PVE-582V
K890969 TRANSESOPHAGEAL TRANSDUCER PEF-511SA
K884555 TCT-600HQ COMPU TOMO(CT)XRAY/HEAD/WHOLE BODY EXAM
K884788 TOSHIBA TCT-600XT COMPUTED TOMOGRAPHY X-RAY SYSTEM
K883359 DIAGNOSTIC ULTRASOUND SYSTEM SSA-270A
K883756 TOSHIBA MRT-50A MAGNETIC RESONANCE SYSTEM
Search all 54 clearances from Toshiba Medical Systems →