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BioCardia 8F Morph DNA Deflectable Guide Catheter

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K192774
510(k) Type
Special
Applicant
Biocardia
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/7/2020
Days to Decision
99 days
Submission Type
Summary

BioCardia 8F Morph DNA Deflectable Guide Catheter

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K192774
510(k) Type
Special
Applicant
Biocardia
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/7/2020
Days to Decision
99 days
Submission Type
Summary