Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA PMA

Pulse generator, pacemaker, implantable, with cardiac resynchronization (CRT-P)

PMA Number: P030005 · 2026-10-03

ApplicantGuidant Corp.
Decision Date2026-10-03
PMA NumberP030005
Product CodeNKE
Device ClassClass 3
Medical SpecialtyU
Advisory CommitteeCV

Device Summary

Pulse generator, pacemaker, implantable, with cardiac resynchronization (CRT-P) is the device name listed in this FDA 510(k) record. The listed applicant is Guidant Corp.. It received FDA 510(k) clearance on 2026-10-03. The device is classified under product code NKE. It was reviewed by the CV advisory panel.

Frequently Asked Questions

What is the Pulse generator, pacemaker, implantable, with cardiac resynchronization (CRT-P)?

Pulse generator, pacemaker, implantable, with cardiac resynchronization (CRT-P) is a medical device that received FDA 510(k) clearance on 2026-10-03. The listed applicant is Guidant Corp..

When did Pulse generator, pacemaker, implantable, with cardiac resynchronization (CRT-P) receive FDA 510(k) clearance?

The clearance date for Pulse generator, pacemaker, implantable, with cardiac resynchronization (CRT-P) can be found in the official FDA records.

Who is the listed applicant for Pulse generator, pacemaker, implantable, with cardiac resynchronization (CRT-P)?

The FDA 510(k) record lists Guidant Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Pulse generator, pacemaker, implantable, with cardiac resynchronization (CRT-P)?

The FDA product code for Pulse generator, pacemaker, implantable, with cardiac resynchronization (CRT-P) is NKE.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT04745156A Study Using Brain Stimulation and Behavioral Therapy to Increase Extent of Resection in Low-Grade GliomasNOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDED

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

↑