PCWNot classified

Implantable Pulse Generator, Programmer And Battery Charger

Unknown

PCW is the FDA product code for Implantable Pulse Generator, Programmer And Battery Charger. FDA's definition for this code reads: "intended for the treatment of moderate to severe heart failure". As of 2026-09-10, FDA records hold no 510(k) clearances under this code and no recalls.

Classification record

Product code: PCW
Device name: Implantable Pulse Generator, Programmer And Battery Charger
FDA definition: intended for the treatment of moderate to severe heart failure.
Device class: Not classified
Review panel: Unknown
Submission type: Contact ODE
Implant: Yes
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 PCW.

Recent clearances

Product code PCW

FDA records hold no clearances under product code PCW.

Recent recalls

Product code PCW

FDA records show no recalls under product code PCW.

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)