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RESPONSE(TM) STEERABLE CATHETER

Page Type
Cleared 510(K)
510(k) Number
K913940
510(k) Type
Traditional
Applicant
DAIG CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/26/1993
Days to Decision
511 days
Submission Type
Statement

RESPONSE(TM) STEERABLE CATHETER

Page Type
Cleared 510(K)
510(k) Number
K913940
510(k) Type
Traditional
Applicant
DAIG CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/26/1993
Days to Decision
511 days
Submission Type
Statement