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FDA 510(k)

Z6 STIMULATOR

K-Number: K070743 · 2007-07-02

ApplicantSt Cardio Technologies, LLC
Decision Date2007-07-02
Product CodeJOQ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Z6 STIMULATOR is the device name listed in this FDA 510(k) record. The listed applicant is St Cardio Technologies, LLC. It received FDA 510(k) clearance on 2007-07-02 under 510(k) number K070743. The device is classified under product code JOQ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Z6 STIMULATOR?

Z6 STIMULATOR is a medical device that received FDA 510(k) clearance on 2007-07-02. The listed applicant is St Cardio Technologies, LLC. The 510(k) number is K070743.

When did Z6 STIMULATOR receive FDA 510(k) clearance?

Z6 STIMULATOR received FDA 510(k) clearance on 2007-07-02, under 510(k) number K070743.

Who is the listed applicant for Z6 STIMULATOR?

The FDA 510(k) record lists St Cardio Technologies, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Z6 STIMULATOR?

The FDA product code for Z6 STIMULATOR is JOQ.

Related Clinical Trials

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Related Devices (Code: JOQ)

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.

K173439Bloom2 Programmable Electrophysiology StimulatorFischer MedicalK092913EP-4TM CARDIAC STIMULATOR, MODELS: EP-04-02, EP-04-04Ep MedsystemsK072200STIMLABMicropace Pty, Ltd.K041442EP-4 CLINICAL STIMUTATOREp MedsystemsK040207EP-4 CLINICAL STIMULATOREp MedsystemsK011826EPS320 CARDIAC STIMULATORMicropace Pty, Ltd.

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.

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