Last synced on 14 November 2025 at 11:06 pm

EVENT MASTER

Page Type
Cleared 510(K)
510(k) Number
K812920
510(k) Type
Traditional
Applicant
INSTRUMENTS FOR CARDIAC RESEARCH
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/2/1981
Days to Decision
44 days

EVENT MASTER

Page Type
Cleared 510(K)
510(k) Number
K812920
510(k) Type
Traditional
Applicant
INSTRUMENTS FOR CARDIAC RESEARCH
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/2/1981
Days to Decision
44 days