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)

TABLE, MASSAGE & TREATMHNT, FIXED HEIGHT

K-Number: K770609 · 1977-04-08

ApplicantWill Ross Co.
Decision Date1977-04-08
Product CodeINT
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

TABLE, MASSAGE & TREATMHNT, FIXED HEIGHT is the device name listed in this FDA 510(k) record. The listed applicant is Will Ross Co.. It received FDA 510(k) clearance on 1977-04-08 under 510(k) number K770609. The device is classified under product code INT. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TABLE, MASSAGE & TREATMHNT, FIXED HEIGHT?

TABLE, MASSAGE & TREATMHNT, FIXED HEIGHT is a medical device that received FDA 510(k) clearance on 1977-04-08. The listed applicant is Will Ross Co.. The 510(k) number is K770609.

When did TABLE, MASSAGE & TREATMHNT, FIXED HEIGHT receive FDA 510(k) clearance?

TABLE, MASSAGE & TREATMHNT, FIXED HEIGHT received FDA 510(k) clearance on 1977-04-08, under 510(k) number K770609.

Who is the listed applicant for TABLE, MASSAGE & TREATMHNT, FIXED HEIGHT?

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

What is the FDA product code for TABLE, MASSAGE & TREATMHNT, FIXED HEIGHT?

The FDA product code for TABLE, MASSAGE & TREATMHNT, FIXED HEIGHT is INT.

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.

Other records listing Will Ross Co. 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.

View all 14 devices →

Related Devices (Code: INT)

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.

↑