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

FDA 510(k) Number Submission Date Device Name Applicant
K051599 06/16/2005 NEURORECOVERY, INC. (NRI) COMPREHENSIVE INTRACRANIAL PRESSURE EVALUATION AND RELIEF (CIPER) KIT NEURORECOVERY, INC.
K022638 08/08/2002 NEURORECOVERY VENTRICULAR CATHETER & MAIN VALVE ASSEMBLY KIT NEURORECOVERY, INC.


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