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CROSSLEAD Penetration Peripheral Guide Wire

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K230377
510(k) Type
Special
Applicant
ASAHI INTECC Co., Ltd.
Country
Japan
FDA Decision
Substantially Equivalent
Decision Date
7/20/2023
Days to Decision
157 days
Submission Type
Summary

CROSSLEAD Penetration Peripheral Guide Wire

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K230377
510(k) Type
Special
Applicant
ASAHI INTECC Co., Ltd.
Country
Japan
FDA Decision
Substantially Equivalent
Decision Date
7/20/2023
Days to Decision
157 days
Submission Type
Summary