FDA.reportPublic FDA data

Device Listing 1778833448

Listing Summary#

Listing key
1778833448
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