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Accipiolx

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K201310
510(k) Type
Traditional
Applicant
MaxQ Al Ltd.
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
8/7/2020
Days to Decision
84 days
Submission Type
Summary

Accipiolx

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K201310
510(k) Type
Traditional
Applicant
MaxQ Al Ltd.
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
8/7/2020
Days to Decision
84 days
Submission Type
Summary