FDA.reportPublic FDA data

Device Listing 2049071897

Listing Summary#

Listing key
2049071897
Premarket submission
K102666
Device
KIMBERLY-CLARK SURGICAL DRAPES WITH AAMI LIQUID BARRIER LEVEL 4 CLAIM
Applicant
Kimberly-Clark Corp.
Product code
KKX
Decision date
2010-11-09