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

Blue Rhino G1-Multi Percutaneous Tracheostomy Introducer Set, Blue Rhino G1-Multi Percutaneous Tracheostomy Introducer Tray, Blue Rhino G2-Multi Percutaneous Tracheostomy Introducer Set, Blue Rhino G2-Multi Percutaneous Tracheostomy Introducer Tray, Weinmann-Multi Percutaneous Tracheostomy Exchange Set

K Number: K193133 · Decision Dec 12, 2019
Classifications
1
FEI Numbers
75
Registration Numbers
75
Same Product Code
108
Applicant Total
175
Review Days
30

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Basic Information

Device Name
Blue Rhino G1-Multi Percutaneous Tracheostomy Introducer Set, Blue Rhino G1-Multi Percutaneous Tracheostomy Introducer Tray, Blue Rhino G2-Multi Percutaneous Tracheostomy Introducer Set, Blue Rhino G2-Multi Percutaneous Tracheostomy Introducer Tray, Weinmann-Multi Percutaneous Tracheostomy Exchange Set
K Number
K193133
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
868.5800
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Cook Incorporated
Date Received
November 12, 2019
Decision Date
December 12, 2019
Product Code
JOH
Advisory Committee
Anesthesiology
Review Advisory Committee
AN
Third Party
N

Classifications

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

Product Code Device Name
JOH Tube Tracheostomy And Tube Cuff

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