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ANGEION IGITAL ANGEFLATOR

Page Type
Cleared 510(K)
510(k) Number
K921757
510(k) Type
Traditional
Applicant
ANGEION CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/18/1993
Days to Decision
339 days
Submission Type
Statement

ANGEION IGITAL ANGEFLATOR

Page Type
Cleared 510(K)
510(k) Number
K921757
510(k) Type
Traditional
Applicant
ANGEION CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/18/1993
Days to Decision
339 days
Submission Type
Statement