Last synced on 2 December 2022 at 11:04 pm

D Camera Controller

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K211332
510(k) Type
Traditional
Applicant
Richard Wolf Medical Instruments Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/1/2021
Days to Decision
151 days
Submission Type
Summary

D Camera Controller

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K211332
510(k) Type
Traditional
Applicant
Richard Wolf Medical Instruments Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/1/2021
Days to Decision
151 days
Submission Type
Summary