510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K980627Substantially Equivalent

Neva System

Urometrics, Inc., St. Paul MN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K980627 is the FDA 510(k) clearance record for NEVA SYSTEM, cleared for Urometrics, Inc. on under FDA product code LIL (Monitor, Penile Tumescence). FDA records list 3 510(k) clearances for Urometrics, Inc., from to . As of , FDA records show no recalls naming K980627.

Clearance record

Decision date
Received
(48 days to decision)
Product code
LIL Monitor, Penile Tumescence
Device class
Unclassified
Review panel
Unknown
Applicant
Urometrics, Inc. 445 Etna St., Suite 56, St. Paul MN
510(k) summary
Summary
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