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Q-CHECK REAGENT STANDARDS

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K830134
510(k) Type
Traditional
Applicant
LAB ABILITY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/9/1983
Days to Decision
0 days

Q-CHECK REAGENT STANDARDS

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K830134
510(k) Type
Traditional
Applicant
LAB ABILITY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/9/1983
Days to Decision
0 days