KRFClass I

Charger, Pacemaker

21 CFR 870.3670 / Cardiovascular

KRF is the FDA product code for Charger, Pacemaker, a class I device type, regulated under 21 CFR 870.3670. As of 2026-09-10, FDA records hold no 510(k) clearances under this code and no recalls.

Classification record

Product code: KRF
Device name: Charger, Pacemaker
Regulation: 21 CFR 870.3670
Device class: Class I
Review panel: Cardiovascular
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

Amphenol DC Electronics

Recent clearances

Product code KRF

FDA records hold no clearances under product code KRF.

Recent recalls

Product code KRF

FDA records show no recalls under product code KRF.

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)