# K070792: Qlab Quantification

- Pathway: 510(k) (Traditional)
- Applicant: Philips Ultrasound, Inc.
- Decided: Apr 6, 2007 after 15 days
- Product code: LLZ (System, Image Processing, Radiological)
- Device class: 2
- Regulation: 21 CFR 892.2050
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
202 later devices descend from it; 6 cite it directly.
0 of 203 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) TomTec 4D MV-Assessment software: named in the summary without a submission number
- (no number) GE Healthcare AFI software: named in the summary without a submission number

## Most influential descendants
- K121223: Qlab with FHN and VPQ Plug-in (2012), 98 descendants of its own
- K120525: Qlab Quantification Software (2012), 92 descendants of its own
- K132165: Qlab Quantification Software (2013), 91 descendants of its own
- K162094: RS80A Diagnostic Ultrasound System (2016), 64 descendants of its own
- K163691: HS70A Diagnostic Ultrasound System (2017), 58 descendants of its own

## Indications for use
QLAB Quantification software is a software application package. It is designed to view and quantify image data acquired on Philips Medical Systems ultrasound products.

Source page: https://510kreport.com/device/K070792
Methodology: https://510kreport.com/methodology