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LYME-SPOT IF KIT

Page Type
Cleared 510(K)
510(k) Number
K910230
510(k) Type
Traditional
Applicant
VITEK SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/30/1991
Days to Decision
224 days

LYME-SPOT IF KIT

Page Type
Cleared 510(K)
510(k) Number
K910230
510(k) Type
Traditional
Applicant
VITEK SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/30/1991
Days to Decision
224 days