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

KIMBERLY CLARK PURPLE NITRILE, AND PURPLE NITRILE XTRA POWDER FREE EXAM GLOVE

K Number: K113423 · Decision Mar 9, 2012
Classifications
1
FEI Numbers
444
Registration Numbers
445
Same Product Code
1158
Applicant Total
104
Review Days
109

Basic Information

Device Name
KIMBERLY CLARK PURPLE NITRILE, AND PURPLE NITRILE XTRA POWDER FREE EXAM GLOVE
K Number
K113423
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
880.6250
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
KIMBERLY-CLARK CORP.
Date Received
November 21, 2011
Decision Date
March 9, 2012
Product Code
LZA
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
Y

Classifications

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

Product Code Device Name
LZA Polymer Patient Examination Glove

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Other Clearances by KIMBERLY-CLARK CORP.

K Number Device Name
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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
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. →