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

INTRAFLON, INTRAFLUX, INTRAVALVE

K Number: K813144 · Decision Nov 27, 1981
Classifications
1
FEI Numbers
23
Registration Numbers
23
Same Product Code
24
Applicant Total
20
Review Days
22

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Basic Information

Device Name
INTRAFLON, INTRAFLUX, INTRAVALVE
K Number
K813144
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1300
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Exco, Inc.
Date Received
November 5, 1981
Decision Date
November 27, 1981
Product Code
DQR
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

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

Product Code Device Name
DQR Cannula, Catheter

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Other Clearances by Exco, Inc.

K Number Device Name
K844203 ENTERNAL FEEDING TUBE SILICONE-EF401, 402 & 403
K844175 ENTERNAL FEEDING TUBE-POLYURETHANE EF504
K844174 FLEXIBLE STAINLESS STEEL STYLET FOR ENTERNAL FEEDI
K832628 VYGON THORACIC DRAINAGE-VARIOUS #'S
K831802 LIFE VAC #2191 & 2192
K833079 CENTRACATH #130,135 & 137-HEMOCATH #
K830910 MANOMETER SET C.V.P. #S 298/299
K822879 ENTERAL NUTRITION 1
K822691 VYGON EPIDURAL ANAESTHESIA TRAY
K822836 MICROFLEX-VENOFLUX
Search all 20 clearances from Exco, Inc. →