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FDA 510(k)

TAICHI STICK MASSAGER

K-Number: K912512 · 1991-09-06

ApplicantFocus International, Inc.
Decision Date1991-09-06
Product CodeLYG
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

TAICHI STICK MASSAGER is the device name listed in this FDA 510(k) record. The listed applicant is Focus International, Inc.. It received FDA 510(k) clearance on 1991-09-06 under 510(k) number K912512. 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 TAICHI STICK MASSAGER?

TAICHI STICK MASSAGER is a medical device that received FDA 510(k) clearance on 1991-09-06. The listed applicant is Focus International, Inc.. The 510(k) number is K912512.

When did TAICHI STICK MASSAGER receive FDA 510(k) clearance?

TAICHI STICK MASSAGER received FDA 510(k) clearance on 1991-09-06, under 510(k) number K912512.

Who is the listed applicant for TAICHI STICK MASSAGER?

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

What is the FDA product code for TAICHI STICK MASSAGER?

The FDA product code for TAICHI STICK 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.K924315THE MASSAGERFour Directions

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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