FDA 510(k) FDA class 2 Unknown 🇺🇸 United States

CONTINUOUS ARTERIAL/VENOUS HEMOFILTRATION TRAY

K Number: K880775 · Decision Jul 25, 1988
Classifications
1
FEI Numbers
6
Registration Numbers
6
Same Product Code
15
Applicant Total
41
Review Days
150

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Basic Information

Device Name
CONTINUOUS ARTERIAL/VENOUS HEMOFILTRATION TRAY
K Number
K880775
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5540
Medical Specialty
Gastroenterology, Urology
Decision
Unknown
Applicant
Medsurg Industries, Inc.
Date Received
February 26, 1988
Decision Date
July 25, 1988
Product Code
LFK
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
N

Classifications

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

Product Code Device Name
LFK Catheter, Femoral

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Other Clearances by Medsurg Industries, Inc.

K Number Device Name
K920780 MEDSURG INSERTION TRAY
K940175 MEDSURG STERILE O.R. TOWELS
K934731 MEDSURG STERILE IMAGING PRODUCTS
K925558 INFILTUBE
K934971 STERILE LAPAROTOMY SPONGES
K920421 MEDSURG MARSHMALLOW TRAY
K920838 MEDSURG CIRCUMCISION TRAY
K931932 DRESSING CHANGE TRAY-MODIFIED
K914037 MEDSURG O.R. PROCEDURE TRAY
K914036 MEDSURG LAPAROSCOPY TRAY
Search all 41 clearances from Medsurg Industries, Inc. →