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RT2 RIGIDITY AND TUMESCENCE TEST

Page Type
Cleared 510(K)
510(k) Number
K925931
510(k) Type
Traditional
Applicant
COMPASS MEDICAL TECHNOLOGIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/21/1992
Days to Decision
28 days
Submission Type
Statement

RT2 RIGIDITY AND TUMESCENCE TEST

Page Type
Cleared 510(K)
510(k) Number
K925931
510(k) Type
Traditional
Applicant
COMPASS MEDICAL TECHNOLOGIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/21/1992
Days to Decision
28 days
Submission Type
Statement