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SAILOR PLUS PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY (PTA) CATHETER, MODEL SAEXXXXXXXXX

Page Type
Cleared 510(K)
510(k) Number
K042538
510(k) Type
Traditional
Applicant
INVATEC INNOVATIVE TECHNOLOGIES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/8/2004
Days to Decision
49 days
Submission Type
Summary

SAILOR PLUS PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY (PTA) CATHETER, MODEL SAEXXXXXXXXX

Page Type
Cleared 510(K)
510(k) Number
K042538
510(k) Type
Traditional
Applicant
INVATEC INNOVATIVE TECHNOLOGIES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/8/2004
Days to Decision
49 days
Submission Type
Summary