Last synced on 20 December 2024 at 11:05 pm

REX, VERSION 3.0

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K030457
510(k) Type
Traditional
Applicant
POINTDX, INC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/8/2003
Days to Decision
56 days
Submission Type
Summary

REX, VERSION 3.0

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K030457
510(k) Type
Traditional
Applicant
POINTDX, INC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/8/2003
Days to Decision
56 days
Submission Type
Summary