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ILLUSION STEERABLE MICROGUIDEWIRE FOR NEUROVAC USE

Page Type
Cleared 510(K)
510(k) Number
K930982
510(k) Type
Traditional
Applicant
CORDIS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/24/1994
Days to Decision
364 days
Submission Type
Summary

ILLUSION STEERABLE MICROGUIDEWIRE FOR NEUROVAC USE

Page Type
Cleared 510(K)
510(k) Number
K930982
510(k) Type
Traditional
Applicant
CORDIS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/24/1994
Days to Decision
364 days
Submission Type
Summary