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HIVOX DREAMATE DM-800

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K021952
510(k) Type
Traditional
Applicant
HIVOX BIOTEK, INC.
Country
Taiwan
FDA Decision
Substantially Equivalent
Decision Date
5/2/2003
Days to Decision
323 days
Submission Type
Statement

HIVOX DREAMATE DM-800

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K021952
510(k) Type
Traditional
Applicant
HIVOX BIOTEK, INC.
Country
Taiwan
FDA Decision
Substantially Equivalent
Decision Date
5/2/2003
Days to Decision
323 days
Submission Type
Statement