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FDA 510(k)

KAVO KEY LASER 1242 AND KAVO KEY LASER 1243+

K-Number: K030146 · 2005-08-03

ApplicantKavo America
Decision Date2005-08-03
Product CodeNVK
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

KAVO KEY LASER 1242 AND KAVO KEY LASER 1243+ is the device name listed in this FDA 510(k) record. The listed applicant is Kavo America. It received FDA 510(k) clearance on 2005-08-03 under 510(k) number K030146. The device is classified under product code NVK. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KAVO KEY LASER 1242 AND KAVO KEY LASER 1243+?

KAVO KEY LASER 1242 AND KAVO KEY LASER 1243+ is a medical device that received FDA 510(k) clearance on 2005-08-03. The listed applicant is Kavo America. The 510(k) number is K030146.

When did KAVO KEY LASER 1242 AND KAVO KEY LASER 1243+ receive FDA 510(k) clearance?

KAVO KEY LASER 1242 AND KAVO KEY LASER 1243+ received FDA 510(k) clearance on 2005-08-03, under 510(k) number K030146.

Who is the listed applicant for KAVO KEY LASER 1242 AND KAVO KEY LASER 1243+?

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

What is the FDA product code for KAVO KEY LASER 1242 AND KAVO KEY LASER 1243+?

The FDA product code for KAVO KEY LASER 1242 AND KAVO KEY LASER 1243+ is NVK.

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Other records listing Kavo America 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.

K073074KEY LASER III 1243 US WITH DETECTK072262GENTLERAY 980 DIODE LASER SYSTEMK063624KAVO EVEREST C-TEMPK051909DIAGNODENTK050019IN EXAM INTRAORAL DENTAL X-RAY SYSTEMK032081KAVO EVEREST ZS-BLANK MODELS, 42, 20, AND 60

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Related Devices (Code: NVK)

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.

K253309SOGA Lasers therapy system family of Aurora handpiece (Aurora-S); SOGA Lasers therapy system family of the Dental diode laser ( ILaser III Pro)Shenzhen Soga Technology Co., Ltd.K260765Gemini NOVA 810+980 Soft Tissue LaserAzena Medical, LLCK250731MateLaser Medical Diode Laser Systems (ML-DLS-30)Matelaser, Inc.K243764Medical Diode Laser (UTU3-F7B,UTU3-F7W,UTU3-G7B,UTU3-G7W,UTU-G20B,UTU-G20W)Wuhan Pioon Technology Co., Ltd.K230047Medical Diode Laser SystemsGigaalaser Company , Ltd.K232885Dawn Diode Laser SystemShanghai Wonderful Opto-Electrics Tech.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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