FDA 510(k) FDA class 2 Substantially Equivalent 🇬🇧 United Kingdom

PORTEX BLUE LINE SACETT SUCTION ABOVE THE CUFF TRACHEAL TUBE, SIZE 6.0 AND 6.5, 7.0 AND 7.5, 8.0 AND 8.5, 9.0

K Number: K081086 · Decision Aug 13, 2008
Classifications
1
FEI Numbers
132
Registration Numbers
132
Same Product Code
240
Applicant Total
52
Review Days
119

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Basic Information

Device Name
PORTEX BLUE LINE SACETT SUCTION ABOVE THE CUFF TRACHEAL TUBE, SIZE 6.0 AND 6.5, 7.0 AND 7.5, 8.0 AND 8.5, 9.0
K Number
K081086
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5730
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Smiths Medical Asd, Inc.
Date Received
April 16, 2008
Decision Date
August 13, 2008
Product Code
BTR
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
BTR Tube, Tracheal (W/Wo Connector)

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K172800 Portex® Lancet Point Spinal Needles with NRFit™ connectors, Portex® Pencil Point Spinal Needles with NRFit™ connectors
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K172410 Portex NRFit Epidural Needles, Portex NRFit Spinal Needles, Portex NRFit Loss of Resistance (L.O.R.) Syringes., Portex EpiFuse Catheter Connector, Portex Regional Anaesthesia Portfolio Filters
K172592 CADD Yellow High Volume Administration Set with NRFit connector
K173912 BLUperc Percutaneous Dilation Tracheostomy Kit with BLUselect tube, BLUperc Percutaneous Dilation Tracheostomy Kit with BLUselect Suctionaid tube, BLUgriggs Percutaneous Dilation Tracheostomy Kit with BLUselect tube, BLUgriggs Percutaneous Dilation Tracheostomy Kit with BLUselect Suctionaid tube
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