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NOVA 13 SODIUM/POTASSIUM/CHLORIDE/LITHIUM ANALYZER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K872190
510(k) Type
Traditional
Applicant
NOVA BIOMEDICAL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/24/1987
Days to Decision
16 days

NOVA 13 SODIUM/POTASSIUM/CHLORIDE/LITHIUM ANALYZER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K872190
510(k) Type
Traditional
Applicant
NOVA BIOMEDICAL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/24/1987
Days to Decision
16 days