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MEVATRON KD-2

Page Type
Cleared 510(K)
510(k) Number
K862339
510(k) Type
Traditional
Applicant
SIEMENS MEDICAL LABORATORIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/29/1986
Days to Decision
131 days

MEVATRON KD-2

Page Type
Cleared 510(K)
510(k) Number
K862339
510(k) Type
Traditional
Applicant
SIEMENS MEDICAL LABORATORIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/29/1986
Days to Decision
131 days