FDA 510(k) Applications Submitted by SKLAR CORP.

FDA 510(k) Number Submission Date Device Name Applicant
K091720 06/11/2009 SKLARLITE RIGID STERILIZATION CONTAINER SYSTEM SKLAR CORP.
K082479 08/28/2008 SKLAR SURGICAL GOWN SKLAR CORP.


Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact