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

KIMBERLY-CLARK INTRODUCER KITS

K Number: K080253 · Decision Feb 26, 2008
Classifications
1
FEI Numbers
25
Registration Numbers
25
Same Product Code
25
Applicant Total
104
Review Days
26

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Basic Information

Device Name
KIMBERLY-CLARK INTRODUCER KITS
K Number
K080253
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
876.5980
Medical Specialty
Gastroenterology, Urology
Decision
Unknown
Statement or Summary
Summary
Applicant
Kimberly-Clark Corp.
Date Received
January 31, 2008
Decision Date
February 26, 2008
Product Code
KGC
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
N

Classifications

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

Product Code Device Name
KGC Tube, Gastro-Enterostomy

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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
K131254 KIMVENT MICROCUFF SUBGLOTTIC SUCTIONING ENDOTRACHEAL TUBE
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
Search all 104 clearances from Kimberly-Clark Corp. →