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

STERILE DESIGN

K Number: K934688 · Decision Mar 16, 1994
Classifications
1
FEI Numbers
159
Registration Numbers
159
Same Product Code
109
Applicant Total
10
Review Days
167

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Basic Information

Device Name
STERILE DESIGN
K Number
K934688
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4370
Medical Specialty
General, Plastic Surgery
Decision
Unknown
Statement or Summary
Summary
Applicant
Sterile Design, Inc.
Date Received
September 30, 1993
Decision Date
March 16, 1994
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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K Number Device Name
K841960 CARDIO METRICS INVASIVE PRESSURE MONIT
K842356 CUSTOM STERILE PROCEDURE KITS
K841959 CARDIO METRIC CUSTOM PERFUSION TUBING
K841958 CARDIO METRICS CARDIOTOMY RESERVOIR
K842351 STERILE DESIGN-CUSTOM STERILE IV KIT
K834239 SDI C-FLEX STERILE LIGHT HANDLE
K834237 GRADUATED GUIDE WIRE BOWL 8
K813437 PAN SET
K791738 CUSTOM DRESSING CHANGE TRAYS