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

DIATEK 600 THERMOMETER SYSTEM

K Number: K833568 · Decision Jan 10, 1984
Classifications
1
FEI Numbers
488
Registration Numbers
488
Same Product Code
797
Applicant Total
15
Review Days
90

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Basic Information

Device Name
DIATEK 600 THERMOMETER SYSTEM
K Number
K833568
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.2910
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Diatek, Inc.
Date Received
October 12, 1983
Decision Date
January 10, 1984
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)
K895703 DIATEK MODEL 700 THERMOMETER
K872178 MODIFICATION TO ARKIVE(TM)
K862085 ARKIVE (TM)
K841827 ENTEROPORT NUTRITION PUMP
K841859 SECURA SET
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. →