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CALIBRATION SOLUTION 1, MODEL A943-837; CALIBRATION SOLUTION 2, MODEL A943-839; RINSE SOLUTION KIT, MODEL A943-838

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K001484
510(k) Type
Traditional
Applicant
ALKO DIAGNOSTIC CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/19/2000
Days to Decision
39 days
Submission Type
Summary

CALIBRATION SOLUTION 1, MODEL A943-837; CALIBRATION SOLUTION 2, MODEL A943-839; RINSE SOLUTION KIT, MODEL A943-838

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K001484
510(k) Type
Traditional
Applicant
ALKO DIAGNOSTIC CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/19/2000
Days to Decision
39 days
Submission Type
Summary