510(k) Predicate Finder
Find potential predicate devices for your 510(k) submission. Enter a K-number to find all clearances with the same product code, a three-letter product code to browse clearances directly, or search by device name.
General Laparoscopic Power Morcellation Containment System
General, Plastic Surgery
The General Laparoscopic Power Morcellation Containment System is a surgical device intended for use by qualified surgeons as a bag containment system during general laparoscopic procedures to facilitate tissue extraction and/or power morcellation while minimizing the risk of tissue dissemination within the abdominal cavity. It is classified as a Class 2 device under regulation 878.4825, requiring 510(k) premarket notification before marketing, and falls within the General, Plastic Surgery (SU) medical specialty. The product code is PZQ. It is not an implant and is not life-sustaining.
510(k) Clearances
1 matchesWhat is a Predicate Device?
A predicate device is a legally marketed device that a new 510(k) applicant uses to demonstrate substantial equivalence. The FDA's 510(k) pathway requires manufacturers to show that their device has the same intended use and similar technological characteristics as one or more predicate devices already cleared for commercial distribution.
Finding the right predicate is a critical step in 510(k) strategy. Manufacturers typically search for cleared devices with the same FDA product code, which groups devices by their intended use and regulatory classification. This tool helps you identify potential predicates by browsing all clearances within a product code.
Note that predicate devices must be legally marketed — they cannot be devices that were cleared but never commercialized, or devices subject to a mandatory recall. The determination of substantial equivalence considers intended use, technological characteristics, and performance data.