Medical Device Manufacturer · US , Mchenry , IL

Kimberly-Clark Corp. - FDA 510(k) Cleared Devices

104 submissions · 103 cleared · Since 1978
Official Website
104
Total
103
Cleared
0
Denied
FDA 510(k) Regulatory Record - Kimberly-Clark Corp. Anesthesiology ✕
3 devices
1-3 of 3
Cleared Aug 20, 2013
KIMVENT MICROCUFF SUBGLOTTIC SUCTIONING ENDOTRACHEAL TUBE
K131254 · BTR
Anesthesiology · 110d
Cleared Dec 19, 2012
KIMVENT MICROCUFF SUBGLOTTIC SUCTIONING
K120985 · BTR
Anesthesiology · 261d
Cleared Apr 22, 2008
MICROCUFF PEDIATRIC ENDOTRACHEAL TUBE
K080821 · BTR
Anesthesiology · 29d
Filters
Filter by Specialty
All104 General Hospital 54 Obstetrics & Gynecology 34 General & Plastic Surgery 7 Gastroenterology & Urology 5 Anesthesiology 3 Cardiovascular 1