FDA 510(k) FDA unclassified Substantially Equivalent 🇺🇸 United States

MICROLIFE DIGITAL BASAL THERMOMETER, MODEL MT 1921

K Number: K030961 · Decision Sep 12, 2003
Classifications
1
FEI Numbers
31
Registration Numbers
31
Same Product Code
23
Applicant Total
13
Review Days
169

Basic Information

Device Name
MICROLIFE DIGITAL BASAL THERMOMETER, MODEL MT 1921
K Number
K030961
Device Class
FDA unclassified
Clearance Type
Traditional
Medical Specialty
Unknown
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
MICROLIFE CORP.
Date Received
March 27, 2003
Decision Date
September 12, 2003
Product Code
LHD
Advisory Committee
Unknown
Review Advisory Committee
OB
Third Party
N

Classifications

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

Product Code Device Name
LHD Device, Fertility Diagnostic, Proceptive

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K Number Device Name
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K080337 MICROLIFE UPPER ARM AUTOMATIC DIGITAL BLOOD PRESSURE MONITOR, MODEL BP3MQ1-2D
K073398 MICROLIFE WRIST WATCH BLOOD PRESSURE MONITOR, MODEL BP3MK1-3 (BP W100)
K073397 MICROLIFE UPPER ARM MANUAL BLOOD PRESSURE MONITOR, MODEL BP3MR1-H (BP A50)
K041411 MICROLIFE UPPER ARM BLOOD PRESSURE MONITOR, MODEL BP-3BTO-AP
K031024 MICROLIFE ELECTRONIC PEAK FLOW MONITOR, MODEL PF-100
K021305 MICROLIFE WRIST WATCH BLOOD PRESSURE, MODEL BP-3BU1-5, WITH OPTIONAL THERMAL PRINTER
K020725 MICROLIFE DIGITAL INFRARED EAR THERMOMETER, MODEL IR1DE1
K013485 MICROLIFE UPPER ARM AUTOMATIC BLOOD PRESSURE MONITOR, MODEL BP-3BTO-1, WITH OPTIONAL THERMAL PRINTER, MODEL PR 1KA1
K003308 MICROLIFE DIGITAL INFRARED EAR THERMOMETER, IR1DAI, IR1DB1, IR1DD1
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