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KYOTEST UGK

Page Type
Cleared 510(K)
510(k) Number
K840829
510(k) Type
Traditional
Applicant
KYOTO DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/19/1984
Days to Decision
55 days

KYOTEST UGK

Page Type
Cleared 510(K)
510(k) Number
K840829
510(k) Type
Traditional
Applicant
KYOTO DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/19/1984
Days to Decision
55 days