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

CATHETER, INTRAVASCULAR (ARGYLE IV SK)

K Number: K760760 · Decision Dec 9, 1976
Classifications
1
FEI Numbers
37
Registration Numbers
37
Same Product Code
13
Applicant Total
62
Review Days
66

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Basic Information

Device Name
CATHETER, INTRAVASCULAR (ARGYLE IV SK)
K Number
K760760
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4200
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Sherwood Medical Industries
Date Received
October 4, 1976
Decision Date
December 9, 1976
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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K792014 LANCER L-INA BUFFER, POLYMER, WASH SOLU
K782077 LANCER ICE CUBE
K790523 ARGYLE ESOPHAGEAL STETHOSCOPE
K790196 MONOJECT ARTERIAL BLOOD SAMPLING DEVICE
K790197 REAGENT KIT, LANCER GLUCOSE
K781459 MONOJECT SCALE MAGNIFIER
K781060 MONOJECT ENDOSSEOUS DENTAL IMPLANT
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