HHGClass III

Dilator, Cervical, Vibratory

21 CFR 884.4270 / Obstetrics/Gynecology

HHG is the FDA product code for Dilator, Cervical, Vibratory, a class III device type, regulated under 21 CFR 884.4270. FDA's definition for this code reads: "Call for PMAs to be filed by 12/26/96 per 61 FR 50708 on 9/27/96". As of 2026-09-10, FDA records hold no 510(k) clearances under this code and no recalls.

Classification record

Product code: HHG
Device name: Dilator, Cervical, Vibratory
FDA definition: Call for PMAs to be filed by 12/26/96 per 61 FR 50708 on 9/27/96
Regulation: 21 CFR 884.4270
Device class: Class III
Review panel: Obstetrics/Gynecology
Submission type: PMA
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

No registered establishment in MDM’s records lists product code HHG.

Recent clearances

Product code HHG

FDA records hold no clearances under product code HHG.

Recent recalls

Product code HHG

FDA records show no recalls under product code HHG.

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)