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FDA 510(k)

STIMLAB

K-Number: K072200 · 2007-10-26

ApplicantMicropace Pty, Ltd.
Decision Date2007-10-26
Product CodeJOQ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

STIMLAB is the device name listed in this FDA 510(k) record. The listed applicant is Micropace Pty, Ltd.. It received FDA 510(k) clearance on 2007-10-26 under 510(k) number K072200. 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 STIMLAB?

STIMLAB is a medical device that received FDA 510(k) clearance on 2007-10-26. The listed applicant is Micropace Pty, Ltd.. The 510(k) number is K072200.

When did STIMLAB receive FDA 510(k) clearance?

STIMLAB received FDA 510(k) clearance on 2007-10-26, under 510(k) number K072200.

Who is the listed applicant for STIMLAB?

The FDA 510(k) record lists Micropace Pty, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for STIMLAB?

The FDA product code for STIMLAB is JOQ.

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.

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Other records listing Micropace Pty, Ltd. as applicant

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.

K253088OneStim-DUO Cardiac Stimulator (MP5003-4CO)K011826EPS320 CARDIAC STIMULATOR

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 MedsystemsK070743Z6 STIMULATORSt Cardio Technologies, LLCK041442EP-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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