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PARENCHYMAL BOLT PRESSURE MONITORING KIT

Page Type
Cleared 510(K)
510(k) Number
K981846
510(k) Type
Traditional
Applicant
CAMINO NEUROCARE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/18/1998
Days to Decision
84 days
Submission Type
Statement

PARENCHYMAL BOLT PRESSURE MONITORING KIT

Page Type
Cleared 510(K)
510(k) Number
K981846
510(k) Type
Traditional
Applicant
CAMINO NEUROCARE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/18/1998
Days to Decision
84 days
Submission Type
Statement