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MODIFICATION TO PENTRA 60 AND PENTRA 60C+

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K030144
510(k) Type
Special
Applicant
ABX DIAGNOSTICS
Country
France
FDA Decision
Substantially Equivalent
Decision Date
1/31/2003
Days to Decision
16 days
Submission Type
Summary

MODIFICATION TO PENTRA 60 AND PENTRA 60C+

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K030144
510(k) Type
Special
Applicant
ABX DIAGNOSTICS
Country
France
FDA Decision
Substantially Equivalent
Decision Date
1/31/2003
Days to Decision
16 days
Submission Type
Summary