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 RELAXARE EXERCISE AND MASSAGE UNIT

K-Number: K862411 · 1986-07-09

Decision Date1986-07-09
Product CodeJFB
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

THE RELAXARE EXERCISE AND MASSAGE UNIT is the device name listed in this FDA 510(k) record. The listed applicant is Relaxare Corp.. It received FDA 510(k) clearance on 1986-07-09 under 510(k) number K862411. The device is classified under product code JFB. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THE RELAXARE EXERCISE AND MASSAGE UNIT?

THE RELAXARE EXERCISE AND MASSAGE UNIT is a medical device that received FDA 510(k) clearance on 1986-07-09. The listed applicant is Relaxare Corp.. The 510(k) number is K862411.

When did THE RELAXARE EXERCISE AND MASSAGE UNIT receive FDA 510(k) clearance?

THE RELAXARE EXERCISE AND MASSAGE UNIT received FDA 510(k) clearance on 1986-07-09, under 510(k) number K862411.

Who is the listed applicant for THE RELAXARE EXERCISE AND MASSAGE UNIT?

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

What is the FDA product code for THE RELAXARE EXERCISE AND MASSAGE UNIT?

The FDA product code for THE RELAXARE EXERCISE AND MASSAGE UNIT is JFB.

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.

Related Devices (Code: JFB)

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.

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.

↑