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AESCULAP SPIEGELBERG BRAIN PRESSURE MONITOR

Page Type
Cleared 510(K)
510(k) Number
K003759
510(k) Type
Traditional
Applicant
AESCULAP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/28/2001
Days to Decision
204 days
Submission Type
Summary

AESCULAP SPIEGELBERG BRAIN PRESSURE MONITOR

Page Type
Cleared 510(K)
510(k) Number
K003759
510(k) Type
Traditional
Applicant
AESCULAP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/28/2001
Days to Decision
204 days
Submission Type
Summary