510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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QAGClass II

Endoscopic Electrosurgical Clip Cutting System

21 CFR 876.4310 / Obstetrics/Gynecology
FDA source (opens on fda.gov)

QAG is the FDA product code for Endoscopic Electrosurgical Clip Cutting System, a class II device type, regulated under 21 CFR 876.4310. FDA's definition for this code reads: "To fragment metallic clips and remove them from the digestive tract". As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and no recalls.

Classification record

Product code
QAG
Device name
Endoscopic Electrosurgical Clip Cutting System
FDA definition
To fragment metallic clips and remove them from the digestive tract.
Regulation
21 CFR 876.4310
Device class
Class II
Review panel
Obstetrics/Gynecology
Submission type
510(k)
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
1
Ingested recalls
0

Clearances, product code QAG

By decision year
1 clearance under product code QAG with a decision year between 2017 and 2017, 2017 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code QAG by decision year
YearClearances
20171

Applicants with the most clearances

Product code QAG
Applicants holding the most 510(k) clearances under product code QAG
ApplicantClearances
Ovesco Endoscopy AG1

Companies listing this code with FDA

Companies whose registered establishments list this code