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CROSSLEAD Peripheral Guide Wire

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K213315
510(k) Type
Traditional
Applicant
Asahi Intecc Co., LTD.
Country
Japan
FDA Decision
Substantially Equivalent
Decision Date
7/1/2022
Days to Decision
270 days
Submission Type
Summary

CROSSLEAD Peripheral Guide Wire

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K213315
510(k) Type
Traditional
Applicant
Asahi Intecc Co., LTD.
Country
Japan
FDA Decision
Substantially Equivalent
Decision Date
7/1/2022
Days to Decision
270 days
Submission Type
Summary