FDA 510(k) K962175, PORTEX ADJUSTABLE FLANGE TRACHEOSTOMY TUBE, by Smiths Industries Medical Systems, Inc.
FDA 510(k) K962175, PORTEX ADJUSTABLE FLANGE TRACHEOSTOMY TUBE, by Smiths Industries Medical Systems, Inc.
Device Classification Name: Tube Tracheostomy And Tube Cuff
510(k) Number: K962175
Device Name: PORTEX ADJUSTABLE FLANGE TRACHEOSTOMY TUBE
Applicant: Smiths Industries Medical Systems, Inc.
Regulation Number: 868.58
Classification Product Code: JOH
Date Received: 1996-06-05
Decision Date: 1997-01-17
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: Anesthesiology
510k Review Panel: Anesthesiology
Total number of pages: 147
Fully redacted pages: 61
Content pages: 86
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