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

MICROFLEX-VENOFLUX

K Number: K822836 · Decision Oct 15, 1982
Classifications
1
FEI Numbers
424
Registration Numbers
424
Same Product Code
1173
Applicant Total
20
Review Days
24

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Basic Information

Device Name
MICROFLEX-VENOFLUX
K Number
K822836
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5440
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Exco, Inc.
Date Received
September 21, 1982
Decision Date
October 15, 1982
Product Code
FPA
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
FPA Set, Administration, Intravascular

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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
K822724 SUCTION TUBES
Search all 20 clearances from Exco, Inc. →