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

MEDSURG MYELOGRAM TRAY

K Number: K880693 · Decision May 11, 1988
Classifications
1
FEI Numbers
548
Registration Numbers
548
Same Product Code
747
Applicant Total
41
Review Days
79

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Basic Information

Device Name
MEDSURG MYELOGRAM TRAY
K Number
K880693
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5860
Medical Specialty
General Hospital
Decision
Unknown
Applicant
Medsurg Industries, Inc.
Date Received
February 22, 1988
Decision Date
May 11, 1988
Product Code
FMF
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
FMF Syringe, Piston

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Other Clearances by Medsurg Industries, Inc.

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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. →