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
K252471Substantially Equivalent

Paptizer 360

Liviliti Health Products Corp, Lake City FL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K252471 is the FDA 510(k) clearance record for Paptizer 360, a class II device, cleared for LiViliti Health Products Corporation on under FDA product code QXQ (Respiratory Accessory Microbial Reduction Device.). FDA's definition for product code QXQ reads: "A respiratory accessory microbial reduction device is a home-use device intended to be used as an adjunct for microbial reduction of compatible respiratory accessories,such as hoses and masks,after cleaning. This device is not intended to...". FDA records list one 510(k) clearance for LiViliti Health Products Corporation. As of , FDA records show no recalls naming K252471.

Clearance record

Decision date
Received
(266 days to decision)
Product code
QXQ Respiratory Accessory Microbial Reduction Device.
Regulation
21 CFR 880.6993
Device class
Class II
Review panel
General Hospital
Applicant
LiViliti Health Products Corporation 2140 SW Main Blvd., Lake City FL
510(k) summary
Summary PDF
Third party review
No

Clearances, product code QXQ

Trailing 12 months
1 clearance under product code QXQ in the twelve months to October 2026, April 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code QXQ, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20261
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260