Last synced on 14 November 2025 at 11:06 pm

Rapid

Page Type
Cleared 510(K)
510(k) Number
K233582
510(k) Type
Traditional
Applicant
iSchema View Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/22/2024
Days to Decision
172 days
Submission Type
Summary

Rapid

Page Type
Cleared 510(K)
510(k) Number
K233582
510(k) Type
Traditional
Applicant
iSchema View Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/22/2024
Days to Decision
172 days
Submission Type
Summary