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

DIATEK MODEL 700 THERMOMETER

K Number: K895703 · Decision Dec 7, 1989
Classifications
1
FEI Numbers
488
Registration Numbers
488
Same Product Code
797
Applicant Total
15
Review Days
76

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Basic Information

Device Name
DIATEK MODEL 700 THERMOMETER
K Number
K895703
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.2910
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Diatek, Inc.
Date Received
September 22, 1989
Decision Date
December 7, 1989
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 Diatek, Inc.

K Number Device Name
K020430 DIATEK CONNECTOR ASSEMBLY REPLACEMENT KIT (CARK)
K010399 DIATEK CANNON-CATH #CC2400, CC2800, CC3200, CC3600,CC5500. CC2400PC, CC2800PC, CC3200PC(32 CM), CC3200PC(36 CM)
K872178 MODIFICATION TO ARKIVE(TM)
K862085 ARKIVE (TM)
K841827 ENTEROPORT NUTRITION PUMP
K841859 SECURA SET
K833568 DIATEK 600 THERMOMETER SYSTEM
K830565 SECURA SET SECONDARY ADMIN. SET
K830377 SECURA SET PRIMARY ADMIN. SET
K830355 SECURA IV VOLUMETRIC INFUSION PUMP
Search all 15 clearances from Diatek, Inc. →