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LYME-CHECK(TM) TEST KIT

Page Type
Cleared 510(K)
510(k) Number
K896378
510(k) Type
Traditional
Applicant
DIAGNOSTIC TECHNOLOGY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/5/1991
Days to Decision
729 days

LYME-CHECK(TM) TEST KIT

Page Type
Cleared 510(K)
510(k) Number
K896378
510(k) Type
Traditional
Applicant
DIAGNOSTIC TECHNOLOGY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/5/1991
Days to Decision
729 days