FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

KIMLON BEDGARD UNDERPAD

K Number: K790384 · Decision Apr 10, 1979
Classifications
1
FEI Numbers
79
Registration Numbers
79
Same Product Code
221
Applicant Total
104
Review Days
43

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Basic Information

Device Name
KIMLON BEDGARD UNDERPAD
K Number
K790384
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
880.5090
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Kimberly-Clark Corp.
Date Received
February 26, 1979
Decision Date
April 10, 1979
Product Code
KMF
Advisory Committee
General Hospital
Review Advisory Committee
SU
Third Party
N

Classifications

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

Product Code Device Name
KMF Bandage, Liquid

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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. →