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THE CROSSER S6 CATHETER, THE CROSSER SYSTEM ELECTRONICS, MODEL CRUS6, GEN200

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K092175
510(k) Type
Traditional
Applicant
Flowcardia, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/17/2010
Days to Decision
211 days
Submission Type
Summary

THE CROSSER S6 CATHETER, THE CROSSER SYSTEM ELECTRONICS, MODEL CRUS6, GEN200

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K092175
510(k) Type
Traditional
Applicant
Flowcardia, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/17/2010
Days to Decision
211 days
Submission Type
Summary