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FDA 510(k)

THE MASSAGER

K-Number: K924315 · 1993-10-08

ApplicantFour Directions
Decision Date1993-10-08
Product CodeLYG
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

THE MASSAGER is the device name listed in this FDA 510(k) record. The listed applicant is Four Directions. It received FDA 510(k) clearance on 1993-10-08 under 510(k) number K924315. The device is classified under product code LYG. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THE MASSAGER?

THE MASSAGER is a medical device that received FDA 510(k) clearance on 1993-10-08. The listed applicant is Four Directions. The 510(k) number is K924315.

When did THE MASSAGER receive FDA 510(k) clearance?

THE MASSAGER received FDA 510(k) clearance on 1993-10-08, under 510(k) number K924315.

Who is the listed applicant for THE MASSAGER?

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

What is the FDA product code for THE MASSAGER?

The FDA product code for THE MASSAGER is LYG.

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Related Devices (Code: LYG)

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.

K963704MUSCLE WAND, A DEVICE FOR DEEP PRESSURE MUSCLE MASSAGEShippert Medical Technologies Corp.K936312MANUAL MASSAGE ROLLERMckenna & CuneoK952043BACK MASSAGEREight Corners, Inc.K930613HOOKING SYSTEMAlain MachtelinckxK936148STRESS HANDLERArocep Enterprises , Ltd.K922366SPINE LINEDambrecine, Inc.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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