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

SPUNGUARD PLUS SURGICAL DRAPE

K Number: K862801 · Decision Aug 7, 1986
Classifications
1
FEI Numbers
200
Registration Numbers
200
Same Product Code
449
Applicant Total
104
Review Days
15

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Basic Information

Device Name
SPUNGUARD PLUS SURGICAL DRAPE
K Number
K862801
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4370
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Kimberly-Clark Corp.
Date Received
July 23, 1986
Decision Date
August 7, 1986
Product Code
KKX
Advisory Committee
General, Plastic Surgery
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
KKX Drape, Surgical, Antimicrobial

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Other Clearances by Kimberly-Clark Corp.

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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. →