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CATHETER, INTRACRANIAL PRESS. MONITOR.

Page Type
Cleared 510(K)
510(k) Number
K772063
510(k) Type
Traditional
Applicant
CORDIS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/3/1978
Days to Decision
62 days

CATHETER, INTRACRANIAL PRESS. MONITOR.

Page Type
Cleared 510(K)
510(k) Number
K772063
510(k) Type
Traditional
Applicant
CORDIS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/3/1978
Days to Decision
62 days