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

MEDSURG O.R. PROCEDURE TRAY

K Number: K914037 · Decision Jun 22, 1993
Classifications
1
FEI Numbers
159
Registration Numbers
159
Same Product Code
109
Applicant Total
41
Review Days
651

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Basic Information

Device Name
MEDSURG O.R. PROCEDURE TRAY
K Number
K914037
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4370
Medical Specialty
General, Plastic Surgery
Decision
Unknown
Statement or Summary
Statement
Applicant
Medsurg Industries, Inc.
Date Received
September 10, 1991
Decision Date
June 22, 1993
Product Code
LRO
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

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

Product Code Device Name
LRO General Surgery Tray

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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
K914036 MEDSURG LAPAROSCOPY TRAY
K893938 CONTINUOUS EPIDURAL ANESTHESIA TRAY
Search all 41 clearances from Medsurg Industries, Inc. →