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ULTRA LYTE POTASSIUM REAGENT KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K843454
510(k) Type
Traditional
Applicant
ULTRA QUEST DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/27/1984
Days to Decision
83 days

ULTRA LYTE POTASSIUM REAGENT KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K843454
510(k) Type
Traditional
Applicant
ULTRA QUEST DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/27/1984
Days to Decision
83 days