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FDA 510(k)

MANUAL MASSAGE ROLLER

K-Number: K936312 · 1996-01-29

ApplicantMckenna & Cuneo
Decision Date1996-01-29
Product CodeLYG
Advisory CommitteePM
DecisionSubstantially Equivalent for Some Indications

Device Summary

MANUAL MASSAGE ROLLER is the device name listed in this FDA 510(k) record. The listed applicant is Mckenna & Cuneo. It received FDA 510(k) clearance on 1996-01-29 under 510(k) number K936312. The device is classified under product code LYG. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the MANUAL MASSAGE ROLLER?

MANUAL MASSAGE ROLLER is a medical device that received FDA 510(k) clearance on 1996-01-29. The listed applicant is Mckenna & Cuneo. The 510(k) number is K936312.

When did MANUAL MASSAGE ROLLER receive FDA 510(k) clearance?

MANUAL MASSAGE ROLLER received FDA 510(k) clearance on 1996-01-29, under 510(k) number K936312.

Who is the listed applicant for MANUAL MASSAGE ROLLER?

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

What is the FDA product code for MANUAL MASSAGE ROLLER?

The FDA product code for MANUAL MASSAGE ROLLER is LYG.

Related Clinical Trials

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Other records listing Mckenna & Cuneo 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.

K971257VTU-1 VACUUM ERECTION SYSTEMK944547DANTEC KEYPOINT

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.K952043BACK MASSAGEREight Corners, Inc.K930613HOOKING 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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