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OMNI DIAGNOST

Page Type
Cleared 510(K)
510(k) Number
K874113
510(k) Type
Traditional
Applicant
XRE CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/16/1987
Days to Decision
38 days

OMNI DIAGNOST

Page Type
Cleared 510(K)
510(k) Number
K874113
510(k) Type
Traditional
Applicant
XRE CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/16/1987
Days to Decision
38 days