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FDA 510(k)

VITALON MATRESS MASSAGE MODEL M-MX

K-Number: K890923 · 1989-03-14

ApplicantNexus Co. , Ltd. C/O Yama Trans Co. , Ltd.
Decision Date1989-03-14
Product CodeISA
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

VITALON MATRESS MASSAGE MODEL M-MX 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 1989-03-14 under 510(k) number K890923. 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 MATRESS MASSAGE MODEL M-MX?

VITALON MATRESS MASSAGE MODEL M-MX is a medical device that received FDA 510(k) clearance on 1989-03-14. The listed applicant is Nexus Co. , Ltd. C/O Yama Trans Co. , Ltd.. The 510(k) number is K890923.

When did VITALON MATRESS MASSAGE MODEL M-MX receive FDA 510(k) clearance?

VITALON MATRESS MASSAGE MODEL M-MX received FDA 510(k) clearance on 1989-03-14, under 510(k) number K890923.

Who is the listed applicant for VITALON MATRESS MASSAGE MODEL M-MX?

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 MATRESS MASSAGE MODEL M-MX?

The FDA product code for VITALON MATRESS MASSAGE MODEL M-MX 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.

K890643VITALON CHAIR MASSAGER MODEL V-CHR2K874843VITALON MASSAGER

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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