GBYClass I

Catheter, Eustachian, General & Plastic Surgery

21 CFR 878.4200 / General, Plastic Surgery

GBY is the FDA product code for Catheter, Eustachian, General & Plastic Surgery, a class I device type, regulated under 21 CFR 878.4200. As of 2026-09-10, FDA records hold no 510(k) clearances under this code and no recalls.

Classification record

Product code: GBY
Device name: Catheter, Eustachian, General & Plastic Surgery
Regulation: 21 CFR 878.4200
Device class: Class I
Review panel: General, Plastic Surgery
Submission type: 510(k) exempt
Implant: No
Life sustaining or supporting: No
GMP exempt: No
Third party review eligible: No
Ingested clearances: 0
Ingested recalls: 0

Companies listing this code with FDA

Companies whose registered establishments list this code

Recent clearances

Product code GBY

FDA records hold no clearances under product code GBY.

Recent recalls

Product code GBY

FDA records show no recalls under product code GBY.

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device classification database, ingested from openFDA. The definition, regulation number, device class and review panel are FDA’s own fields, reproduced without editing.

MDM adds the counts: clearances by decision year, the applicants holding the most clearances under this code, recalls that name it, and the registered establishments that list it. Every count is computed from ingested records only.

Data as of 2026-10-05, the FDA export date for this dataset. Page last changed 2026-09-05. View this product code on fda.gov (opens on fda.gov)