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PHASE II LH KIT

Page Type
Cleared 510(K)
510(k) Number
K882252
510(k) Type
Traditional
Applicant
VITEK SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/4/1988
Days to Decision
65 days

PHASE II LH KIT

Page Type
Cleared 510(K)
510(k) Number
K882252
510(k) Type
Traditional
Applicant
VITEK SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/4/1988
Days to Decision
65 days