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 510(k)

THE SIGNATURE SERIES, M IV

K-Number: K933197 · 1995-06-02

ApplicantProgressive Electrical Therapeutics
Decision Date1995-06-02
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

THE SIGNATURE SERIES, M IV is the device name listed in this FDA 510(k) record. The listed applicant is Progressive Electrical Therapeutics. It received FDA 510(k) clearance on 1995-06-02 under 510(k) number K933197. The device is classified under product code GZJ. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THE SIGNATURE SERIES, M IV?

THE SIGNATURE SERIES, M IV is a medical device that received FDA 510(k) clearance on 1995-06-02. The listed applicant is Progressive Electrical Therapeutics. The 510(k) number is K933197.

When did THE SIGNATURE SERIES, M IV receive FDA 510(k) clearance?

THE SIGNATURE SERIES, M IV received FDA 510(k) clearance on 1995-06-02, under 510(k) number K933197.

Who is the listed applicant for THE SIGNATURE SERIES, M IV?

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

What is the FDA product code for THE SIGNATURE SERIES, M IV?

The FDA product code for THE SIGNATURE SERIES, M IV is GZJ.

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 Progressive Electrical Therapeutics 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.

K943972EURO TECH DIAMOND CHIROPRACTIC TABLEK943973EURO TECH STERLING ROLLER TABLEK943975EURO TECH PLATINUM CHIROPRACTIC TABLEK943974EURO TECH MARQUISE CHIROPRACTIC TABLEK933194THE SIGNATURE SERIES, IMC IVK933196THE SIGNATURE SERIES, IC II

View all 10 devices →

Related Devices (Code: GZJ)

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.

K252712STIMPOD NMS460 Nerve StimulatorAlgiamed Technologies USA, Inc.K252767actiTENS miniSublimedK252236CP Relief Wand Rx - TENS/NMESN & C Holdings, LLCK232441Unipro (K-UNIPRO-US)Tenscare, Ltd.K241228TENSWaveZynex Medical OfficerK233046Electrical Neuromuscular Stimulator, Cure TrioOriental Inspiration Limited

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.

↑