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FDA 510(k)

STIMU-TAP

K-Number: K944024 · 1994-12-08

ApplicantWahl Clipper Corp.
Decision Date1994-12-08
Product CodeISA
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

STIMU-TAP 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 1994-12-08 under 510(k) number K944024. 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 STIMU-TAP?

STIMU-TAP is a medical device that received FDA 510(k) clearance on 1994-12-08. The listed applicant is Wahl Clipper Corp.. The 510(k) number is K944024.

When did STIMU-TAP receive FDA 510(k) clearance?

STIMU-TAP received FDA 510(k) clearance on 1994-12-08, under 510(k) number K944024.

Who is the listed applicant for STIMU-TAP?

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 STIMU-TAP?

The FDA product code for STIMU-TAP 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 SERIESK940837WAHL(R) FOOT COMFORT MASSAGERK941412WAHL COMPACT COMFORT MASSAGERK941594WAHL DOUBLE 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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