Last synced on 23 May 2025 at 11:06 pm

KING SODIUM/POTASSIUM STANDARD MODIFIED

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K931834
510(k) Type
Traditional
Applicant
KING DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/25/1993
Days to Decision
152 days
Submission Type
Summary

KING SODIUM/POTASSIUM STANDARD MODIFIED

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K931834
510(k) Type
Traditional
Applicant
KING DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/25/1993
Days to Decision
152 days
Submission Type
Summary