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

MEDSURG CIRCUMCISION TRAY

K Number: K920838 · Decision Oct 15, 1993
Classifications
1
FEI Numbers
0
Registration Numbers
0
Same Product Code
0
Applicant Total
41
Review Days
599

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Basic Information

Device Name
MEDSURG CIRCUMCISION TRAY
K Number
K920838
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
884.3900
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Medsurg Industries, Inc.
Date Received
February 24, 1992
Decision Date
October 15, 1993
Product Code
HFK
Advisory Committee
Obstetrics/Gynecology
Review Advisory Committee
OB
Third Party
N

Classifications

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

Product Code Device Name
HFK Mold, Vaginal

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
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. →