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FDA 510(k)

VITALON MASSAGER

K-Number: K874843 · 1988-01-20

ApplicantNexus Co. , Ltd. C/O Yama Trans Co. , Ltd.
Decision Date1988-01-20
Product CodeISA
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

VITALON MASSAGER is the device name listed in this FDA 510(k) record. The listed applicant is Nexus Co. , Ltd. C/O Yama Trans Co. , Ltd.. It received FDA 510(k) clearance on 1988-01-20 under 510(k) number K874843. The device is classified under product code ISA. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VITALON MASSAGER?

VITALON MASSAGER is a medical device that received FDA 510(k) clearance on 1988-01-20. The listed applicant is Nexus Co. , Ltd. C/O Yama Trans Co. , Ltd.. The 510(k) number is K874843.

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

VITALON MASSAGER received FDA 510(k) clearance on 1988-01-20, under 510(k) number K874843.

Who is the listed applicant for VITALON MASSAGER?

The FDA 510(k) record lists Nexus Co. , Ltd. C/O Yama Trans Co. , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VITALON MASSAGER?

The FDA product code for VITALON MASSAGER 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 Nexus Co. , Ltd. C/O Yama Trans Co. , Ltd. 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.

K890923VITALON MATRESS MASSAGE MODEL M-MXK890643VITALON CHAIR MASSAGER MODEL V-CHR2

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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