Last synced on 14 November 2025 at 11:06 pm

C3 PATIENT MONITOR

Page Type
Cleared 510(K)
510(k) Number
K030931
510(k) Type
Special
Applicant
ANALOGIC CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/9/2003
Days to Decision
45 days
Submission Type
Summary

C3 PATIENT MONITOR

Page Type
Cleared 510(K)
510(k) Number
K030931
510(k) Type
Special
Applicant
ANALOGIC CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/9/2003
Days to Decision
45 days
Submission Type
Summary