Last synced on 23 September 2022 at 11:05 pm

TGDC-01 PRA

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K021937
510(k) Type
Traditional
Applicant
TRUEVISION INSTRUMENTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/11/2002
Days to Decision
121 days
Submission Type
Summary

TGDC-01 PRA

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K021937
510(k) Type
Traditional
Applicant
TRUEVISION INSTRUMENTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/11/2002
Days to Decision
121 days
Submission Type
Summary