Tool · 510(k)

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.

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Describe your device and the Research Assistant searches 510(k)s, compares intended use, and drafts a predicate shortlist — with citations.

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Product Code: LLO FDA class 2

Laser, Neodymium:Yag, Pulmonary Surgery

Ear, Nose, Throat

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Laser, Neodymium:YAG, Pulmonary Surgery is a neodymium-doped yttrium aluminum garnet (Nd:YAG) laser system used in surgical procedures involving the lungs and airways, such as bronchoscopic resection of endobronchial tumors or treatment of tracheobronchial obstructions. It is classified as FDA Class 2, indicating moderate risk, and requires 510(k) premarket clearance. The product code is LLO, regulated under 21 CFR 874.4500, within the Ear, Nose, and Throat medical specialty. This device is eligible for third-party 510(k) review.

510(k) Clearances

19 matches
K Number
Device Name
SLT CLMD CONTACT LASER
SURGILASE YAG 100 FOR GYNECOLOGY USE
LASEGUIDE 600A, 600B, 400A, 400B FOR PULMONARY USE
MODEL 4900 ND:YAG LASER FOR PULMONARY OBSTRUCTIONS
ND:YAG SURGICAL LASER FOR PULMONARY APPLICATIONS
SURGI-LIGHT DISPOSABLE SYSTEM FOR PULMONOLOGY USE
MODEL 5050 SURGILASER FOR PULMONARY USE
FIBERLASE II ND:YAG LASER FOR PULMONARY USE
OPTILASE YAG MODEL 1000 SURG LASER SYS/PULMON APPL
SL-100 ND:YAG LASER FOR PULMONARY OBSTRUCTIONS
6000 ND:YAG LASER FOR BENIGN/MALIGNANT OBSTRUCTION
LASER BRONCHOSCOPE SYSTEM
CO2 LASER BRONCHOSCOPE SYSTEM
MODEL 2100 ND:YAG SURGICAL LASER PULMONARY INDICAT
S.L.T. CONTACT LASER ND:YAG USE IN PULMONARY AIRWA
CILAS MODEL YM101
ND: YAGLASER FOR PALLIATIVE TREAT OF OBSTRUCTION
LASER BENIGN & MALIGNANT PULMONARY OBSTRUCTIONS-
FIBERLASE 100 MEDICAL LASER SYSTEM

What 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.

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