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FDA 510(k)

PHASER (SINGLE LINEAR MECHANICAL MASSAGE)

K-Number: K891871 · 1989-04-25

ApplicantMonad Corp.
Decision Date1989-04-25
Product CodeISA
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

PHASER (SINGLE LINEAR MECHANICAL MASSAGE) is the device name listed in this FDA 510(k) record. The listed applicant is Monad Corp.. It received FDA 510(k) clearance on 1989-04-25 under 510(k) number K891871. 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 PHASER (SINGLE LINEAR MECHANICAL MASSAGE)?

PHASER (SINGLE LINEAR MECHANICAL MASSAGE) is a medical device that received FDA 510(k) clearance on 1989-04-25. The listed applicant is Monad Corp.. The 510(k) number is K891871.

When did PHASER (SINGLE LINEAR MECHANICAL MASSAGE) receive FDA 510(k) clearance?

PHASER (SINGLE LINEAR MECHANICAL MASSAGE) received FDA 510(k) clearance on 1989-04-25, under 510(k) number K891871.

Who is the listed applicant for PHASER (SINGLE LINEAR MECHANICAL MASSAGE)?

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

What is the FDA product code for PHASER (SINGLE LINEAR MECHANICAL MASSAGE)?

The FDA product code for PHASER (SINGLE LINEAR MECHANICAL MASSAGE) is ISA.

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Other records listing Monad Corp. 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.

K914441MENS 2000-DK902226MY-O-MATIC 5000IK904234MENS-O-MATIC IK904258MICRO DERMK904235MENS-O-MATIC 2000K904260MENS-O-MATIC 3000

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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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