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IMPAX DIAGNOSTIC DISPLAY STATION,IMPAX CLINICAL REVIEW STATION,IMPAX FOR CARDIOLOGY CLINICAL REVIEW SATATION,IMPAX ORTHO

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K022292
510(k) Type
Traditional
Applicant
AGFA CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/12/2002
Days to Decision
59 days
Submission Type
Summary

IMPAX DIAGNOSTIC DISPLAY STATION,IMPAX CLINICAL REVIEW STATION,IMPAX FOR CARDIOLOGY CLINICAL REVIEW SATATION,IMPAX ORTHO

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K022292
510(k) Type
Traditional
Applicant
AGFA CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/12/2002
Days to Decision
59 days
Submission Type
Summary