510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K991479Substantially Equivalent

Viser Penile Tumescence Monitor

Laborie Medical Tech Corp., Williston VT / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K991479 is the FDA 510(k) clearance record for VISER PENILE TUMESCENCE MONITOR, cleared for Laborie Medical Tech Corp. on under FDA product code LIL (Monitor, Penile Tumescence). FDA records list 6 510(k) clearances for Laborie Medical Tech Corp., from to . As of , FDA records show no recalls naming K991479.

Clearance record

Decision date
Received
(70 days to decision)
Product code
LIL Monitor, Penile Tumescence
Device class
Unclassified
Review panel
Unknown
Applicant
Laborie Medical Tech Corp. 310 Hurricane Ln. #2, Williston VT
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