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EASYLYTE SODIUM/POTASSIUM/LITHIUM ANALYZER

Page Type
Cleared 510(K)
510(k) Number
K914810
510(k) Type
Traditional
Applicant
MEDICA CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/4/1991
Days to Decision
40 days
Submission Type
Statement

EASYLYTE SODIUM/POTASSIUM/LITHIUM ANALYZER

Page Type
Cleared 510(K)
510(k) Number
K914810
510(k) Type
Traditional
Applicant
MEDICA CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/4/1991
Days to Decision
40 days
Submission Type
Statement