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CRITERION II PACING SYSTEM MONITORS

Page Type
Cleared 510(K)
510(k) Number
K802325
510(k) Type
Traditional
Applicant
DART MEDICAL EQUIPMENT
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/23/1980
Days to Decision
30 days

CRITERION II PACING SYSTEM MONITORS

Page Type
Cleared 510(K)
510(k) Number
K802325
510(k) Type
Traditional
Applicant
DART MEDICAL EQUIPMENT
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/23/1980
Days to Decision
30 days