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

KIMBERLY-CLARK GAS PLASMA STERILIZATION INDICATOR STRIP

K Number: K974415 · Decision Jul 10, 1998
Classifications
1
FEI Numbers
130
Registration Numbers
130
Same Product Code
264
Applicant Total
104
Review Days
228

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Basic Information

Device Name
KIMBERLY-CLARK GAS PLASMA STERILIZATION INDICATOR STRIP
K Number
K974415
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.2800
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Kimberly-Clark Corp.
Date Received
November 24, 1997
Decision Date
July 10, 1998
Product Code
JOJ
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
JOJ Indicator, Physical/Chemical Sterilization Process

Similar 510(k) Clearances

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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. →