FDA 510(k) Applications Submitted by DIANE DAVIS

FDA 510(k) Number Submission Date Device Name Applicant
K961122 03/21/1996 STRYKER KNIFELIGHT STRYKER INSTRUMENTS
K961970 05/20/1996 COMMAND 2 MICOELECTRIC SURGICAL SYSTEM STRYKER CORP.
K962800 07/18/1996 STRYKER UNIVERSAL DRILL ATTACHMENTS & ACCESSORIES STRYKER INSTRUMENTS


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