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LYTENING 6 SODIUM/POTASSIUM/IONIZED CALCIUM ANALYZ

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K884731
510(k) Type
Traditional
Applicant
AMDEV, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/3/1989
Days to Decision
85 days

LYTENING 6 SODIUM/POTASSIUM/IONIZED CALCIUM ANALYZ

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K884731
510(k) Type
Traditional
Applicant
AMDEV, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/3/1989
Days to Decision
85 days