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

KIMGUARD ONE-STEP STERILIZATION WRAP

K Number: K112805 · Decision Jun 22, 2012
Classifications
1
FEI Numbers
194
Registration Numbers
194
Same Product Code
321
Applicant Total
104
Review Days
269

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Basic Information

Device Name
KIMGUARD ONE-STEP STERILIZATION WRAP
K Number
K112805
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.6850
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Kimberly-Clark Corp.
Date Received
September 27, 2011
Decision Date
June 22, 2012
Product Code
FRG
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

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

Product Code Device Name
FRG Wrap, Sterilization

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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
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. →