Last synced on 18 April 2025 at 11:05 pm

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

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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