PLL

Submucosal Injection Agent

Product code
PLL
Device name
Submucosal Injection Agent
Device class
Class 2
21 CFR
21 CFR 876.1500
Medical specialty
Gastroenterology, Urology
Marketing pathway
510(K)
510(k) clearances (last 3 years)
1
Summaries archived here
1 (direct download)
510(k) clearances (all years, FDA)
9 (all years; only the last 3 years are listed here)

FDA classification definition

Intended for use in gastrointestinal endoscopic procedures for submucosal lift of polyps, adenomas, early-stage cancers or other gastrointestinal mucosal lesions, prior to excision with a snare or endoscopic device.

Definition text from the FDA device classification database (U.S. federal government work, public domain).

510(k) clearances, last 3 years (1)

Last three years. Most recent: 2024-07-03.

NumberDecision dateApplicantDevice nameSummary
K2415912024-07-03The Standard Co., Ltd.Blue EyePDF

1 summaries are archived here for direct download.

Official FDA classification page: PLL
Classification and pathway per current FDA publications. Data from openFDA (CC0).