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FDA 510(k)

SWISS MASTER LIGHT

K-Number: K032099 · 2003-10-27

Applicant(Ems Sa) Electro Medical Systems
Decision Date2003-10-27
Product CodeEBZ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

SWISS MASTER LIGHT is the device name listed in this FDA 510(k) record. The listed applicant is (Ems Sa) Electro Medical Systems. It received FDA 510(k) clearance on 2003-10-27 under 510(k) number K032099. The device is classified under product code EBZ. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SWISS MASTER LIGHT?

SWISS MASTER LIGHT is a medical device that received FDA 510(k) clearance on 2003-10-27. The listed applicant is (Ems Sa) Electro Medical Systems. The 510(k) number is K032099.

When did SWISS MASTER LIGHT receive FDA 510(k) clearance?

SWISS MASTER LIGHT received FDA 510(k) clearance on 2003-10-27, under 510(k) number K032099.

Who is the listed applicant for SWISS MASTER LIGHT?

The FDA 510(k) record lists (Ems Sa) Electro Medical Systems as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SWISS MASTER LIGHT?

The FDA product code for SWISS MASTER LIGHT is EBZ.

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 (Ems Sa) Electro Medical Systems 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.

K073284AIR-FLOW MASTER STANDARDK992504EMS KERMITK991874EMS SURFACE MOUNT SCALERK991588EMS SWISS ORTHOCLAST

Related Devices (Code: EBZ)

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.

K253131Curing Light (M-Cure 6)Guangzhou Rebornendo Medical Instrument Co., Ltd.K253461Demi ProMeta Systems Co., Ltd.K242386BluemoonGenoss Co., Ltd.K243921LED Curing Lights (DB686 HALO)Foshan Coxo Medical Instrument Co., Ltd.K250009LED Curing Light (C01-X, C02-X)Premium Plus (Dongguan) LimitedK241238LOOP™ LED Curing Light System (CLK01)Garrison Dental Solutions, LLC

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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