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

SECURA IV VOLUMETRIC INFUSION PUMP

K Number: K830355 · Decision Mar 1, 1983
Classifications
1
FEI Numbers
149
Registration Numbers
149
Same Product Code
847
Applicant Total
15
Review Days
26

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Basic Information

Device Name
SECURA IV VOLUMETRIC INFUSION PUMP
K Number
K830355
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5725
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Diatek, Inc.
Date Received
February 3, 1983
Decision Date
March 1, 1983
Product Code
FRN
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
FRN Pump, Infusion

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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
K833568 DIATEK 600 THERMOMETER SYSTEM
K830565 SECURA SET SECONDARY ADMIN. SET
K830377 SECURA SET PRIMARY ADMIN. SET
Search all 15 clearances from Diatek, Inc. →