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VXTRA OCUTOME KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K832980
510(k) Type
Traditional
Applicant
VXTRA CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/19/1983
Days to Decision
47 days

VXTRA OCUTOME KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K832980
510(k) Type
Traditional
Applicant
VXTRA CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/19/1983
Days to Decision
47 days