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BLUE LINE(R) PDT(TM) PORTEX DIRECTIONAL TUBE

Page Type
Cleared 510(K)
510(k) Number
K931735
510(k) Type
Traditional
Applicant
SMITHS INDUSTRIES MEDICAL SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/18/1993
Days to Decision
41 days
Submission Type
Summary

BLUE LINE(R) PDT(TM) PORTEX DIRECTIONAL TUBE

Page Type
Cleared 510(K)
510(k) Number
K931735
510(k) Type
Traditional
Applicant
SMITHS INDUSTRIES MEDICAL SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/18/1993
Days to Decision
41 days
Submission Type
Summary