510(K) CLEARANCES 51 ▲2RECALLS POSTED 25 ▲2CLASS I 1PMA DECISIONS 50 ▲13WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K110414Substantially Equivalent

Qlab 8.1 Quantification Software

Philips North America LLC, Bothell WA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K110414 is the FDA 510(k) clearance record for QLAB 8.1 QUANTIFICATION SOFTWARE, a class II device, cleared for Philips Ultrasound, Inc. on under FDA product code LLZ (System, Image Processing, Radiological). FDA records list 680 510(k) clearances for Philips North America LLC, from to . As of , FDA records show no recalls naming K110414.

Clearance record

Decision date
Received
(127 days to decision)
Product code
LLZ System, Image Processing, Radiological
Regulation
21 CFR 892.2050
Device class
Class II
Review panel
Radiology
Applicant
Philips Ultrasound, Inc. 22100 Bothell Everett Hwy., Bothell WA
510(k) summary
Summary PDF
Third party review
Yes

Clearances, product code LLZ

Trailing 12 months
46 clearances under product code LLZ in the twelve months to November 2026, July 2026 the highest month at 8.
Show the numbers
Monthly 510(k) clearances under FDA product code LLZ, trailing twelve months
MonthClearances
December 20251
January 20263
February 20264
March 20266
April 20262
May 20265
June 20265
July 20268
August 20263
September 20267
October 20262
November 20260