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CAL 1 AND CAL 2 STANDARDS/STANDARDS FOR IL 501 SODIUM/POTASSIUM ANALYZER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K935547
510(k) Type
Traditional
Applicant
ALKO DIAGNOSTIC CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/18/1994
Days to Decision
62 days
Submission Type
Summary

CAL 1 AND CAL 2 STANDARDS/STANDARDS FOR IL 501 SODIUM/POTASSIUM ANALYZER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K935547
510(k) Type
Traditional
Applicant
ALKO DIAGNOSTIC CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/18/1994
Days to Decision
62 days
Submission Type
Summary