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

KIMVENT MICROCUFF SUBGLOTTIC SUCTIONING ENDOTRACHEAL TUBE

K Number: K131254 · Decision Aug 20, 2013
Classifications
1
FEI Numbers
132
Registration Numbers
132
Same Product Code
240
Applicant Total
104
Review Days
110

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Basic Information

Device Name
KIMVENT MICROCUFF SUBGLOTTIC SUCTIONING ENDOTRACHEAL TUBE
K Number
K131254
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5730
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Kimberly-Clark Corp.
Date Received
May 2, 2013
Decision Date
August 20, 2013
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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Other Clearances by Kimberly-Clark Corp.

K Number Device Name
K140963 KIMGUARD SMART-FOLD STERILIZATION WRAP
K141294 U BY KOTEX SECURITY UNSCENTED MENSTRUAL TAMPONS
K131879 KC 300 SURGICAL MASK
K131841 KIMBERLY-CLARK LAVENDER NITRILE POWDER-FREE EXAM GLOVE
K120985 KIMVENT MICROCUFF SUBGLOTTIC SUCTIONING
K112805 KIMGUARD ONE-STEP STERILIZATION WRAP
K113423 KIMBERLY CLARK PURPLE NITRILE, AND PURPLE NITRILE XTRA POWDER FREE EXAM GLOVE
K112300 KIMGUARD SMART-FOLD* STERILIZATION WRAP
K112635 U BY KOTEX SLEEK UNSCENTED MENSTRUAL TAMPONS
K110455 KIMBERLY-CLARK LOW BARRIER, ASTM 2100 FACE MASKS
Search all 104 clearances from Kimberly-Clark Corp. →