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DIGISCOPE RX-2

Page Type
Cleared 510(K)
510(k) Number
K960198
510(k) Type
Traditional
Applicant
MEDIREX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/12/1996
Days to Decision
56 days
Submission Type
Statement

DIGISCOPE RX-2

Page Type
Cleared 510(K)
510(k) Number
K960198
510(k) Type
Traditional
Applicant
MEDIREX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/12/1996
Days to Decision
56 days
Submission Type
Statement