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FDA 510(k)

RELAXY-WONDER KNOCK

K-Number: K950320 · 1995-02-14

ApplicantKinsei Shiatsu, Inc.
Decision Date1995-02-14
Product CodeISA
Advisory CommitteePM
DecisionSubstantially Equivalent for Some Indications

Device Summary

RELAXY-WONDER KNOCK is the device name listed in this FDA 510(k) record. The listed applicant is Kinsei Shiatsu, Inc.. It received FDA 510(k) clearance on 1995-02-14 under 510(k) number K950320. The device is classified under product code ISA. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the RELAXY-WONDER KNOCK?

RELAXY-WONDER KNOCK is a medical device that received FDA 510(k) clearance on 1995-02-14. The listed applicant is Kinsei Shiatsu, Inc.. The 510(k) number is K950320.

When did RELAXY-WONDER KNOCK receive FDA 510(k) clearance?

RELAXY-WONDER KNOCK received FDA 510(k) clearance on 1995-02-14, under 510(k) number K950320.

Who is the listed applicant for RELAXY-WONDER KNOCK?

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

What is the FDA product code for RELAXY-WONDER KNOCK?

The FDA product code for RELAXY-WONDER KNOCK is ISA.

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.

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Other records listing Kinsei Shiatsu, Inc. 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.

K952990SPIN ROLLEREK952916SHIATSU MASTER MASSAGER CUSHIONK950411RELAXU-1K950322RELAXY-THE WONDER HANDK950321SHAPE UP MOMI ROLLER

Related Devices (Code: ISA)

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.

K243488VMAT PROTermosaludK240358ShockPhysio Mobile (model SW3200 Basic)Shenzhen Dongdixin Technology Co., Ltd.K221865BTL-094BTL Industries, Inc.K210166Omnispec ED1000Medispec, Ltd.K213120OW100S (model OW100S-US)Tissue Regeneration Technologies, LLC Dba AS Softwave TrtK220538DolorClast RadialE.M.S Electro Medical Systems S.A

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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