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LITHIUM INTERNAL STANDARD 1 MEQ/L #60085

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K871185
510(k) Type
Traditional
Applicant
IN VITRO DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/28/1987
Days to Decision
65 days

LITHIUM INTERNAL STANDARD 1 MEQ/L #60085

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K871185
510(k) Type
Traditional
Applicant
IN VITRO DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/28/1987
Days to Decision
65 days