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FDA 510(k)

AVON MASSAGING HAIRBRUSH

K-Number: K950931 · 1995-04-05

ApplicantSiegel,Mandell & Davidson,P.C.
Decision Date1995-04-05
Product CodeISA
Advisory CommitteePM
DecisionSubstantially Equivalent for Some Indications

Device Summary

AVON MASSAGING HAIRBRUSH is the device name listed in this FDA 510(k) record. The listed applicant is Siegel,Mandell & Davidson,P.C.. It received FDA 510(k) clearance on 1995-04-05 under 510(k) number K950931. The device is classified under product code ISA. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the AVON MASSAGING HAIRBRUSH?

AVON MASSAGING HAIRBRUSH is a medical device that received FDA 510(k) clearance on 1995-04-05. The listed applicant is Siegel,Mandell & Davidson,P.C.. The 510(k) number is K950931.

When did AVON MASSAGING HAIRBRUSH receive FDA 510(k) clearance?

AVON MASSAGING HAIRBRUSH received FDA 510(k) clearance on 1995-04-05, under 510(k) number K950931.

Who is the listed applicant for AVON MASSAGING HAIRBRUSH?

The FDA 510(k) record lists Siegel,Mandell & Davidson,P.C. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AVON MASSAGING HAIRBRUSH?

The FDA product code for AVON MASSAGING HAIRBRUSH 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 Siegel,Mandell & Davidson,P.C. 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.

K951008POWER RANGERS SUNGLASSESK946091AVON SUNNY DAYS SUNGLASSESK946092AVON SUNNY DAYS SUNGLASSESK941369AVON CAT SUNGLASSES

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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