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FDA 510(k)

FACIAL MASSAGER, BATTERY POWERED

K-Number: K863383 · 1986-09-15

ApplicantGeneral Physiotherapy, Inc.
Decision Date1986-09-15
Product CodeISA
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

FACIAL MASSAGER, BATTERY POWERED is the device name listed in this FDA 510(k) record. The listed applicant is General Physiotherapy, Inc.. It received FDA 510(k) clearance on 1986-09-15 under 510(k) number K863383. 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 FACIAL MASSAGER, BATTERY POWERED?

FACIAL MASSAGER, BATTERY POWERED is a medical device that received FDA 510(k) clearance on 1986-09-15. The listed applicant is General Physiotherapy, Inc.. The 510(k) number is K863383.

When did FACIAL MASSAGER, BATTERY POWERED receive FDA 510(k) clearance?

FACIAL MASSAGER, BATTERY POWERED received FDA 510(k) clearance on 1986-09-15, under 510(k) number K863383.

Who is the listed applicant for FACIAL MASSAGER, BATTERY POWERED?

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

What is the FDA product code for FACIAL MASSAGER, BATTERY POWERED?

The FDA product code for FACIAL MASSAGER, BATTERY POWERED is ISA.

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Other records listing General Physiotherapy, 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.

K870939VIBRACAREK861834THERACUSHION MODEL 1000K855129NEOCUSSOR (MASSAGER, BATTERY) POWEREDK853710THERACUSHIONK852944FLEXIMATIC MASSAGERK850047SANYO ELECTRONIC MUSCLE STIMULATORS

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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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