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LACRYTEST

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K034057
510(k) Type
Traditional
Applicant
ADIATEC SA
Country
France
FDA Decision
Substantially Equivalent
Decision Date
3/9/2004
Days to Decision
70 days
Submission Type
Summary

LACRYTEST

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K034057
510(k) Type
Traditional
Applicant
ADIATEC SA
Country
France
FDA Decision
Substantially Equivalent
Decision Date
3/9/2004
Days to Decision
70 days
Submission Type
Summary