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FDA 510(k)

BACK MASSAGER

K-Number: K952043 · 1995-09-01

ApplicantEight Corners, Inc.
Decision Date1995-09-01
Product CodeLYG
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

BACK MASSAGER is the device name listed in this FDA 510(k) record. The listed applicant is Eight Corners, Inc.. It received FDA 510(k) clearance on 1995-09-01 under 510(k) number K952043. 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 BACK MASSAGER?

BACK MASSAGER is a medical device that received FDA 510(k) clearance on 1995-09-01. The listed applicant is Eight Corners, Inc.. The 510(k) number is K952043.

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

BACK MASSAGER received FDA 510(k) clearance on 1995-09-01, under 510(k) number K952043.

Who is the listed applicant for BACK MASSAGER?

The FDA 510(k) record lists Eight Corners, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BACK MASSAGER?

The FDA product code for BACK MASSAGER is LYG.

Related Clinical Trials

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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 & CuneoK930613HOOKING SYSTEMAlain MachtelinckxK936148STRESS HANDLERArocep Enterprises , Ltd.K924315THE MASSAGERFour DirectionsK922366SPINE LINEDambrecine, Inc.

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.

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