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ANGEION ENDOSCOPIC VALVE SEAL

Page Type
Cleared 510(K)
510(k) Number
K915719
510(k) Type
Traditional
Applicant
ANGEION CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/18/1992
Days to Decision
60 days
Submission Type
Statement

ANGEION ENDOSCOPIC VALVE SEAL

Page Type
Cleared 510(K)
510(k) Number
K915719
510(k) Type
Traditional
Applicant
ANGEION CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/18/1992
Days to Decision
60 days
Submission Type
Statement