Last synced on 14 November 2025 at 11:06 pm

Accipiolx

Page Type
Cleared 510(K)
510(k) Number
K182177
510(k) Type
Traditional
Applicant
MaxQ-Al Ltd.
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
10/26/2018
Days to Decision
77 days
Submission Type
Summary

Accipiolx

Page Type
Cleared 510(K)
510(k) Number
K182177
510(k) Type
Traditional
Applicant
MaxQ-Al Ltd.
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
10/26/2018
Days to Decision
77 days
Submission Type
Summary