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CROSSBOSS CATHETER MODEL M-2000, STINGRAY ORIENTING BALLOON CATHETER MODEL M-1000, STINGRAY GUIDEWIRE MODEL M-3004 AND M

Page Type
Cleared 510(K)
510(k) Number
K102725
510(k) Type
Traditional
Applicant
BRIDGE MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/10/2011
Days to Decision
231 days
Submission Type
Summary

CROSSBOSS CATHETER MODEL M-2000, STINGRAY ORIENTING BALLOON CATHETER MODEL M-1000, STINGRAY GUIDEWIRE MODEL M-3004 AND M

Page Type
Cleared 510(K)
510(k) Number
K102725
510(k) Type
Traditional
Applicant
BRIDGE MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/10/2011
Days to Decision
231 days
Submission Type
Summary