510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K925931Substantially Equivalent

Rt2 Rigidity and Tumescence Test

Compass Medical Technologies, Inc., Minneapolis MN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K925931 is the FDA 510(k) clearance record for RT2 RIGIDITY AND TUMESCENCE TEST, cleared for Compass Medical Technologies, Inc. on under FDA product code LIL (Monitor, Penile Tumescence). FDA records list one 510(k) clearance for Compass Medical Technologies, Inc. As of , FDA records show no recalls naming K925931.

Clearance record

Decision date
Received
(28 days to decision)
Product code
LIL Monitor, Penile Tumescence
Device class
Unclassified
Review panel
Unknown
Applicant
Compass Medical Technologies, Inc. 5005 Bryant Ave. S., Minneapolis MN
510(k) summary
Statement
Third party review
No

Clearances, product code LIL

Trailing 12 months

FDA records hold no clearances under product code LIL in the trailing twelve months.

FDA records show no clearances under product code LIL in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code LIL, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260