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)

BACK MASTER

K-Number: K914394 · 1991-11-13

ApplicantProgressive Electrical Therapeutics
Decision Date1991-11-13
Product CodeBXB
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

BACK MASTER 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 1991-11-13 under 510(k) number K914394. The device is classified under product code BXB. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BACK MASTER?

BACK MASTER is a medical device that received FDA 510(k) clearance on 1991-11-13. The listed applicant is Progressive Electrical Therapeutics. The 510(k) number is K914394.

When did BACK MASTER receive FDA 510(k) clearance?

BACK MASTER received FDA 510(k) clearance on 1991-11-13, under 510(k) number K914394.

Who is the listed applicant for BACK MASTER?

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 BACK MASTER?

The FDA product code for BACK MASTER is BXB.

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.

K933197THE SIGNATURE SERIES, M IVK943972EURO TECH DIAMOND CHIROPRACTIC TABLEK943973EURO TECH STERLING ROLLER TABLEK943974EURO TECH MARQUISE CHIROPRACTIC TABLEK943975EURO TECH PLATINUM CHIROPRACTIC TABLEK933194THE SIGNATURE SERIES, IMC IV

View all 10 devices →

Related Devices (Code: BXB)

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.

K072887G-TRAINER MEDICALAlter-G, Inc.K003272FLO-BOOTDiscovery Group, LLCK952975ANKLE CALF EXERCISER PHLEBOPUMPPrevent Products, Inc.K953456E-Z FLEXFluid Motion Biotechnologies, Inc.K955106BTE CPM-20Baltimore Therapeutic Equipment Co.K955105BTE CPM-10Baltimore Therapeutic Equipment Co.

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.

↑