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FDA 510(k)

WAHL(R) ULTRA COMFORT MASSAGER SPEC #89ISA

K-Number: K940683 · 1994-06-09

ApplicantWahl Clipper Corp.
Decision Date1994-06-09
Product CodeISA
Advisory CommitteePM
DecisionSubstantially Equivalent for Some Indications

Device Summary

WAHL(R) ULTRA COMFORT MASSAGER SPEC #89ISA is the device name listed in this FDA 510(k) record. The listed applicant is Wahl Clipper Corp.. It received FDA 510(k) clearance on 1994-06-09 under 510(k) number K940683. 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 WAHL(R) ULTRA COMFORT MASSAGER SPEC #89ISA?

WAHL(R) ULTRA COMFORT MASSAGER SPEC #89ISA is a medical device that received FDA 510(k) clearance on 1994-06-09. The listed applicant is Wahl Clipper Corp.. The 510(k) number is K940683.

When did WAHL(R) ULTRA COMFORT MASSAGER SPEC #89ISA receive FDA 510(k) clearance?

WAHL(R) ULTRA COMFORT MASSAGER SPEC #89ISA received FDA 510(k) clearance on 1994-06-09, under 510(k) number K940683.

Who is the listed applicant for WAHL(R) ULTRA COMFORT MASSAGER SPEC #89ISA?

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

What is the FDA product code for WAHL(R) ULTRA COMFORT MASSAGER SPEC #89ISA?

The FDA product code for WAHL(R) ULTRA COMFORT MASSAGER SPEC #89ISA is ISA.

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Other records listing Wahl Clipper 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.

K944909WAHL FRESH FACEK950701WAHL SPORTS RELIEF HOT/COLD MASSAGER ROLLERK9461623M(TM) SURGICAL SLIPPER, 9660 SERIESK944024STIMU-TAPK941412WAHL COMPACT COMFORT MASSAGERK940837WAHL(R) FOOT COMFORT MASSAGER

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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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