Last synced on 25 April 2025 at 11:05 pm

AXERA 2 ACCESS SYSTEM MODEL AXE200

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K123135
510(k) Type
Traditional
Applicant
ARSTASIS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/28/2013
Days to Decision
115 days
Submission Type
Summary

AXERA 2 ACCESS SYSTEM MODEL AXE200

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K123135
510(k) Type
Traditional
Applicant
ARSTASIS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/28/2013
Days to Decision
115 days
Submission Type
Summary