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FDA 510(k)

LITESABER 2000

K-Number: K993942 · 2000-01-18

ApplicantLaser Dental Innovations
Decision Date2000-01-18
Product CodeGEX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

LITESABER 2000 is the device name listed in this FDA 510(k) record. The listed applicant is Laser Dental Innovations. It received FDA 510(k) clearance on 2000-01-18 under 510(k) number K993942. The device is classified under product code GEX. It was reviewed by the SU advisory panel. Product code GEX falls under the category of Gastroenterology, which includes gastrointestinal diagnostic and therapeutic devices. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LITESABER 2000?

LITESABER 2000 is a medical device that received FDA 510(k) clearance on 2000-01-18. The listed applicant is Laser Dental Innovations. The 510(k) number is K993942.

When did LITESABER 2000 receive FDA 510(k) clearance?

LITESABER 2000 received FDA 510(k) clearance on 2000-01-18, under 510(k) number K993942.

Who is the listed applicant for LITESABER 2000?

The FDA 510(k) record lists Laser Dental Innovations as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LITESABER 2000?

The FDA product code for LITESABER 2000 is GEX. This falls under the Gastroenterology category.

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 Laser Dental Innovations 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.

K052604STARLITE 2006

Related Devices (Code: GEX)

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.

K254199PicoreMax (PicoreMax)BLUECORE COMPANY Co., Ltd.K252723Dynamis Pro FamilyFotona D.O.O.K241973SmartIPL_NI SystemLumenis Be, Ltd.K261047Dental Diode Laser Device (Laser-Pen)Guilin Kevin Peter Technology Co., Ltd.K261817Diode Laser Therapy System (PZ-BDT67-01, PZ-BDT67-02)Zhengzhou PZ Laser Slim Technology Co., Ltd.K261673LED Therapy Device (QLXY-01)Beijing Nubway S&T Co., Ltd.

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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