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MODEL AM 721 ELECTROLYTE ANALYZER

Page Type
Cleared 510(K)
510(k) Number
K810135
510(k) Type
Traditional
Applicant
ABBOTT DIAGNOSTICS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/10/1981
Days to Decision
20 days

MODEL AM 721 ELECTROLYTE ANALYZER

Page Type
Cleared 510(K)
510(k) Number
K810135
510(k) Type
Traditional
Applicant
ABBOTT DIAGNOSTICS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/10/1981
Days to Decision
20 days