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FDA 510(k)

AQUASSAGER WM110/W210 & WM120 BODY BASICS MASSAGER

K-Number: K925907 · 1994-03-30

ApplicantPollenex Corp.
Decision Date1994-03-30
Product CodeISA
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

AQUASSAGER WM110/W210 & WM120 BODY BASICS MASSAGER is the device name listed in this FDA 510(k) record. The listed applicant is Pollenex Corp.. It received FDA 510(k) clearance on 1994-03-30 under 510(k) number K925907. 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 AQUASSAGER WM110/W210 & WM120 BODY BASICS MASSAGER?

AQUASSAGER WM110/W210 & WM120 BODY BASICS MASSAGER is a medical device that received FDA 510(k) clearance on 1994-03-30. The listed applicant is Pollenex Corp.. The 510(k) number is K925907.

When did AQUASSAGER WM110/W210 & WM120 BODY BASICS MASSAGER receive FDA 510(k) clearance?

AQUASSAGER WM110/W210 & WM120 BODY BASICS MASSAGER received FDA 510(k) clearance on 1994-03-30, under 510(k) number K925907.

Who is the listed applicant for AQUASSAGER WM110/W210 & WM120 BODY BASICS MASSAGER?

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

What is the FDA product code for AQUASSAGER WM110/W210 & WM120 BODY BASICS MASSAGER?

The FDA product code for AQUASSAGER WM110/W210 & WM120 BODY BASICS 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 Pollenex 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.

K925055POLLENEX HEPA AIR CLEANERS

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

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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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