Last synced on 14 November 2025 at 11:06 pm

ECG MODULATOR

Page Type
Cleared 510(K)
510(k) Number
K760563
510(k) Type
Traditional
Applicant
PHYSIO-CONTROL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/10/1976
Days to Decision
8 days

ECG MODULATOR

Page Type
Cleared 510(K)
510(k) Number
K760563
510(k) Type
Traditional
Applicant
PHYSIO-CONTROL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/10/1976
Days to Decision
8 days