510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K052929Substantially Equivalent

Preftest Professional Suite

Limestone Technologies, Inc., Dundas, CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K052929 is the FDA 510(k) clearance record for PREFTEST PROFESSIONAL SUITE, cleared for Limestone Technologies, Inc. on under FDA product code LIL (Monitor, Penile Tumescence). FDA records list one 510(k) clearance for Limestone Technologies, Inc. As of , FDA records show no recalls naming K052929.

Clearance record

Decision date
Received
(189 days to decision)
Product code
LIL Monitor, Penile Tumescence
Device class
Unclassified
Review panel
Unknown
Applicant
Limestone Technologies, Inc. 4 Innovation Dr., Dundas, CA
510(k) summary
Summary PDF
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