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HISTOFREEZER DEVICE

Page Type
Cleared 510(K)
510(k) Number
K990877
510(k) Type
Traditional
Applicant
ORASURE TECHNOLOGIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/14/1999
Days to Decision
90 days
Submission Type
Statement

HISTOFREEZER DEVICE

Page Type
Cleared 510(K)
510(k) Number
K990877
510(k) Type
Traditional
Applicant
ORASURE TECHNOLOGIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/14/1999
Days to Decision
90 days
Submission Type
Statement