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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.
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