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

MEDSURG 16 GA. CENTRAL VEIN CATHETERIZATION TRAY

K Number: K880779 · Decision May 9, 1988
Classifications
1
FEI Numbers
104
Registration Numbers
104
Same Product Code
400
Applicant Total
41
Review Days
73

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Basic Information

Device Name
MEDSURG 16 GA. CENTRAL VEIN CATHETERIZATION TRAY
K Number
K880779
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.4210
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Medsurg Industries, Inc.
Date Received
February 26, 1988
Decision Date
May 9, 1988
Product Code
DWF
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
DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass

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Other Clearances by Medsurg Industries, Inc.

K Number Device Name
K920780 MEDSURG INSERTION TRAY
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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. →