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KNOLL/MIDUS (MALE IMPOTENCE DIAGNOSTIC ULTRASONIC SYSTEM)

Page Type
Cleared 510(K)
510(k) Number
K971790
510(k) Type
Traditional
Applicant
UROMETRICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/17/1997
Days to Decision
217 days
Submission Type
Summary

KNOLL/MIDUS (MALE IMPOTENCE DIAGNOSTIC ULTRASONIC SYSTEM)

Page Type
Cleared 510(K)
510(k) Number
K971790
510(k) Type
Traditional
Applicant
UROMETRICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/17/1997
Days to Decision
217 days
Submission Type
Summary