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

KIMBERLY-CLARK CHILD/PEDIATRIC FACE MASK

K Number: K103150 · Decision Sep 23, 2011
Classifications
1
FEI Numbers
12
Registration Numbers
12
Same Product Code
8
Applicant Total
5
Review Days
332

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
KIMBERLY-CLARK CHILD/PEDIATRIC FACE MASK
K Number
K103150
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4040
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Kimberly-Clark
Date Received
October 26, 2010
Decision Date
September 23, 2011
Product Code
OXZ
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
OXZ Pediatric/Child Facemask

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (OXZ), ordered by most recent decision date.

View all

Other Clearances by Kimberly-Clark

K Number Device Name
K113340 KIMBERLY-CLARK CHILD'S FACEMASK
K112562 BAL CATH BRONCHIAL ASPIRATE SAMPLING CATHETER
K111402 KC200, SURGICAL MASK, KC200, PROCEDURE MASK, KC300, SURGICALMASK, FLUIDSHIELD, KC300, PROCEDURE MASK, FLUIDSHIELD MODEL
K101596 KIMBERLY-CLARK PURPLE NITRILE POWDER-FREE EXAM GLOVE (CHEMOTHERAPY GLOVE) AND KIMBERLY-CLARK PURPLE NITRILE XTRA POWDER-