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

JELCO* DISC FILTER-0.2 MICRON

K Number: K790471 · Decision Apr 30, 1979
Classifications
1
FEI Numbers
50
Registration Numbers
50
Same Product Code
97
Applicant Total
26
Review Days
56

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Basic Information

Device Name
JELCO* DISC FILTER-0.2 MICRON
K Number
K790471
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5440
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Jelco Laboratories
Date Received
March 5, 1979
Decision Date
April 30, 1979
Product Code
FPB
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
FPB Filter, Infusion Line

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Other Clearances by Jelco Laboratories

K Number Device Name
K791918 JELCO WINGED INTRAVASCULAR CATHETER
K791372 JELCO & KVO CATHETER PLACEMENT UNIT
K790967 CATHETER METAL HUB/RADIOPAQUE
K790968 CATHETER METAL HUB/NONRADIOPAQUE
K790186 PROTECTIVSTABILIZER
K790079 NEEDLE, BLOOD COLLECTING
K790107 CATHETER TUBING MODIFICATION
K781857 TRAY, ARTERIAL BLOOD GAS SAMPLING
K780896 NEEDLES, DESIGN CHANGE, IV CATHETERS
K780519 FILTER TUBE
Search all 26 clearances from Jelco Laboratories →