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NEOS 02

Page Type
Cleared 510(K)
510(k) Number
K894240
510(k) Type
Traditional
Applicant
BIOTRONIK CARDIAC PACEMAKERS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/26/1989
Days to Decision
128 days

NEOS 02

Page Type
Cleared 510(K)
510(k) Number
K894240
510(k) Type
Traditional
Applicant
BIOTRONIK CARDIAC PACEMAKERS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/26/1989
Days to Decision
128 days