FDA 510(k) Applications Submitted by SARSTEDT, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K051019 04/22/2005 SAFETY NEEDLE SARSTEDT, INC.
K031359 04/30/2003 S-MONOVETTE EDTA K2-GEL SARSTEDT, INC.
K032150 07/14/2003 SAFETY-MULTIFLY SARSTEDT, INC.
K003382 10/31/2000 SARSTEDT NEEDLE PROTECTOR SARSTEDT, INC.
K024237 12/23/2002 URINE MONOVETTE BORIC ACID SARSTEDT, INC.


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