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

MEDSURG INSERTION TRAY

K Number: K920780 · Decision Aug 19, 1994
Classifications
1
FEI Numbers
23
Registration Numbers
23
Same Product Code
64
Applicant Total
41
Review Days
911

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Basic Information

Device Name
MEDSURG INSERTION TRAY
K Number
K920780
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5540
Medical Specialty
Gastroenterology, Urology
Decision
Unknown
Statement or Summary
Statement
Applicant
Medsurg Industries, Inc.
Date Received
February 20, 1992
Decision Date
August 19, 1994
Product Code
LFJ
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
LFJ Catheter, Subclavian

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Other Clearances by Medsurg Industries, Inc.

K Number Device Name
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
K893938 CONTINUOUS EPIDURAL ANESTHESIA TRAY
Search all 41 clearances from Medsurg Industries, Inc. →