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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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