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LYME IGM MICROASSAY

Page Type
Cleared 510(K)
510(k) Number
K911330
510(k) Type
Traditional
Applicant
DIAMEDIX CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/10/1991
Days to Decision
77 days

LYME IGM MICROASSAY

Page Type
Cleared 510(K)
510(k) Number
K911330
510(k) Type
Traditional
Applicant
DIAMEDIX CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/10/1991
Days to Decision
77 days