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TGDC-01 PRA

Page Type
Cleared 510(K)
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)
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