Product Code: FGX FDA class 1 21 CFR 876.4730

Snare, Non-Electrical

Gastroenterology, Urology

The Non-Electrical Snare is a loop-type instrument used mechanically, without electrical energy, to capture, ligate, or remove tissue polyps or other lesions during gastrointestinal or urological endoscopic procedures. It is classified as FDA Class 1, the lowest risk category, subject only to general controls. The product code is FGX, regulated under 21 CFR 876.4730, within the Gastroenterology, Urology medical specialty.

510(k)s
0
FEI Numbers
53
Registration Numbers
53
Unique Applicants
0
Years Active

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Basic Information

Product Code
FGX
Device Class
FDA class 1
Regulation Number
876.4730
Medical Specialty
Gastroenterology, Urology
Review Panel
GU
Submission Type
4

Device Characteristics

GMP Exempt
Implant
Life Sustain/Support
Third Party
Summary Malfunction Reporting

FEI Numbers

This FDA classification entry is associated with 53 FEI numbers. Click on an entry to view related FDA registrations.

Registration Numbers

This FDA classification entry is associated with 53 registration numbers. Click on an entry to view related FDA registrations.