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VXTRA OCUTOME KIT

Page Type
Cleared 510(K)
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)
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