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TECHNICON AXON TM SYSTEM ADDITIONAL ANALYTES

Page Type
Cleared 510(K)
510(k) Number
K892929
510(k) Type
Traditional
Applicant
TECHNICON INSTRUMENTS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/20/1989
Days to Decision
90 days

TECHNICON AXON TM SYSTEM ADDITIONAL ANALYTES

Page Type
Cleared 510(K)
510(k) Number
K892929
510(k) Type
Traditional
Applicant
TECHNICON INSTRUMENTS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/20/1989
Days to Decision
90 days