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

FDA 510(k) Number Submission Date Device Name Applicant
K072379 08/24/2007 MPS OXIPORT AND MPS OXIPORT PLUS INNERSPACE, INC.
K083378 11/14/2008 SYNERGY INNERSPACE, INC.
K010422 02/12/2001 ACT II ICP MONITORING SYSTEM AND VENTRICULAR CATHETER INNERSPACE, INC.
K041838 07/07/2004 MPS (OR MPS-T) INNERSPACE, INC.
K013005 09/06/2001 ACT 11 MP VENTRICULAR CATHETER INNERSPACE, INC.
K013705 11/08/2001 ACT III VENTRICULAR CATHETER INNERSPACE, INC.
K003905 12/19/2000 ACTI-ICP MONITORING SYSTEM INNERSPACE, INC.


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