Last synced on 14 November 2025 at 11:06 pm

LEAD, SUTURELESS MYOCARDIAL

Page Type
Cleared 510(K)
510(k) Number
K800355
510(k) Type
Traditional
Applicant
DAIG CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/28/1980
Days to Decision
103 days

LEAD, SUTURELESS MYOCARDIAL

Page Type
Cleared 510(K)
510(k) Number
K800355
510(k) Type
Traditional
Applicant
DAIG CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/28/1980
Days to Decision
103 days