Last synced on 23 February 2024 at 11:04 pm

Rapid (6.0)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K233512
510(k) Type
Special
Applicant
iSchemaView, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/16/2024
Days to Decision
76 days
Submission Type
Summary

Rapid (6.0)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K233512
510(k) Type
Special
Applicant
iSchemaView, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/16/2024
Days to Decision
76 days
Submission Type
Summary