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MODEL FT-100 INTRACRANIAL PRESSURE MONITOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K890468
510(k) Type
Traditional
Applicant
PEARL INSTRUMENTS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/26/1989
Days to Decision
85 days

MODEL FT-100 INTRACRANIAL PRESSURE MONITOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K890468
510(k) Type
Traditional
Applicant
PEARL INSTRUMENTS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/26/1989
Days to Decision
85 days