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CORONARY PERIPHERAL AND RENAL STEERABLE GUIDEWIRE

Page Type
Cleared 510(K)
510(k) Number
K042338
510(k) Type
Special
Applicant
LAKE REGION MFG., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/16/2004
Days to Decision
17 days
Submission Type
Summary

CORONARY PERIPHERAL AND RENAL STEERABLE GUIDEWIRE

Page Type
Cleared 510(K)
510(k) Number
K042338
510(k) Type
Special
Applicant
LAKE REGION MFG., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/16/2004
Days to Decision
17 days
Submission Type
Summary