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FDA 510(k)

STIMUPLEX HNS-12, MODEL 4892098

K-Number: K052313 · 2005-11-17

ApplicantStockert GmbH
Decision Date2005-11-17
Product CodeBXN
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

STIMUPLEX HNS-12, MODEL 4892098 is the device name listed in this FDA 510(k) record. The listed applicant is Stockert GmbH. It received FDA 510(k) clearance on 2005-11-17 under 510(k) number K052313. The device is classified under product code BXN. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STIMUPLEX HNS-12, MODEL 4892098?

STIMUPLEX HNS-12, MODEL 4892098 is a medical device that received FDA 510(k) clearance on 2005-11-17. The listed applicant is Stockert GmbH. The 510(k) number is K052313.

When did STIMUPLEX HNS-12, MODEL 4892098 receive FDA 510(k) clearance?

STIMUPLEX HNS-12, MODEL 4892098 received FDA 510(k) clearance on 2005-11-17, under 510(k) number K052313.

Who is the listed applicant for STIMUPLEX HNS-12, MODEL 4892098?

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

What is the FDA product code for STIMUPLEX HNS-12, MODEL 4892098?

The FDA product code for STIMUPLEX HNS-12, MODEL 4892098 is BXN.

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_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Stockert GmbH 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.

K070336STOCKERT NEURO N50, MODEL12267K070134MODIFICATION TO STIMUPLEX HNS-12, MODEL 4892098K061983STIMUPLEX PENK003983STIMUPLEX HNS-11

Related Devices (Code: BXN)

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.

K213049STIMPOD NMS450 Nerve StimulatorXavant Technology (Pty), Ltd.K162086MultiStim ECOPAJUNK GmbH MedizintechnologieK153045SunStim Peripheral Nerve Stimulator/Sunstim Plus Peripheral Nerve StimulatorEasy Med Instrument Co., Ltd.K121743EASYMED PERIPHERAL NERVE STIMULATOR-SUNSTINSunmed, LLCK111985MYOGUIDE SYSTEM MODEL 8008Intronix Technologies Corp.K110118STIMTRODE SINGLE USE NERVE STIMULATORXavant Technology (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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