FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

JELCO & KVO CATHETER PLACEMENT UNIT

K Number: K791372 · Decision Sep 12, 1979
Classifications
1
FEI Numbers
37
Registration Numbers
37
Same Product Code
13
Applicant Total
26
Review Days
50

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Basic Information

Device Name
JELCO & KVO CATHETER PLACEMENT UNIT
K Number
K791372
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4200
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Jelco Laboratories
Date Received
July 24, 1979
Decision Date
September 12, 1979
Product Code
JCY
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

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

Product Code Device Name
JCY Catheter, Infusion

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Other Clearances by Jelco Laboratories

K Number Device Name
K791918 JELCO WINGED INTRAVASCULAR CATHETER
K790967 CATHETER METAL HUB/RADIOPAQUE
K790968 CATHETER METAL HUB/NONRADIOPAQUE
K790471 JELCO* DISC FILTER-0.2 MICRON
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 →