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Cleaner™ Pro Thrombectomy System; Cleaner™ Pro Aspiration Catheter with Handpiece; Cleaner™ Pro Aspiration Canister

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K232679
510(k) Type
Traditional
Applicant
Argon Medical Devices, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/19/2024
Days to Decision
140 days
Submission Type
Summary

Cleaner™ Pro Thrombectomy System; Cleaner™ Pro Aspiration Catheter with Handpiece; Cleaner™ Pro Aspiration Canister

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K232679
510(k) Type
Traditional
Applicant
Argon Medical Devices, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/19/2024
Days to Decision
140 days
Submission Type
Summary