Last synced on 13 December 2024 at 11:05 pm

Rapid ASPECTS (v3)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K232156
510(k) Type
Traditional
Applicant
iSchemaView, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/19/2024
Days to Decision
183 days
Submission Type
Summary

Rapid ASPECTS (v3)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K232156
510(k) Type
Traditional
Applicant
iSchemaView, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/19/2024
Days to Decision
183 days
Submission Type
Summary