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RT2 RIGIDITY AND TUMESCENCE TEST

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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