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PARENCHYMAL BOLT PRESSURE MONITORING KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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