Last synced on 4 February 2023 at 10:33 pm

Primary Relief

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K213188
510(k) Type
Traditional
Applicant
DyAnsys, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/31/2022
Days to Decision
124 days
Submission Type
Summary

Primary Relief

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K213188
510(k) Type
Traditional
Applicant
DyAnsys, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/31/2022
Days to Decision
124 days
Submission Type
Summary