Last synced on 23 May 2025 at 11:06 pm

ALKO CALIBRATORS AND FLUSH SOLUTION FOR IL 1300 SERIES PH/BLOOD GAS ANALYZERS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K945966
510(k) Type
Traditional
Applicant
ALKO DIAGNOSTIC CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/10/1995
Days to Decision
65 days
Submission Type
Summary

ALKO CALIBRATORS AND FLUSH SOLUTION FOR IL 1300 SERIES PH/BLOOD GAS ANALYZERS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K945966
510(k) Type
Traditional
Applicant
ALKO DIAGNOSTIC CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/10/1995
Days to Decision
65 days
Submission Type
Summary