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FDA 510(k)

BELMONT UNIT, MODEL 2000 SERIES

K-Number: K000799 · 2000-05-17

ApplicantBelmont Equipment Corp.
Decision Date2000-05-17
Product CodeEIA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

BELMONT UNIT, MODEL 2000 SERIES is the device name listed in this FDA 510(k) record. The listed applicant is Belmont Equipment Corp.. It received FDA 510(k) clearance on 2000-05-17 under 510(k) number K000799. The device is classified under product code EIA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BELMONT UNIT, MODEL 2000 SERIES?

BELMONT UNIT, MODEL 2000 SERIES is a medical device that received FDA 510(k) clearance on 2000-05-17. The listed applicant is Belmont Equipment Corp.. The 510(k) number is K000799.

When did BELMONT UNIT, MODEL 2000 SERIES receive FDA 510(k) clearance?

BELMONT UNIT, MODEL 2000 SERIES received FDA 510(k) clearance on 2000-05-17, under 510(k) number K000799.

Who is the listed applicant for BELMONT UNIT, MODEL 2000 SERIES?

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

What is the FDA product code for BELMONT UNIT, MODEL 2000 SERIES?

The FDA product code for BELMONT UNIT, MODEL 2000 SERIES is EIA.

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Other records listing Belmont Equipment 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.

K983661BELMONT UNIT, MODEL 6000 SERIES AND 7500 SERIESK963699BELRAY/MODEL 096, DENTAL INTRAORAL X-RAYK900681PANORAMIC MODEL X-CALIBER X-RAYK874238MODEL 2001 CP, PHOTON I, DENTAL, INTRAORAL X-RAYK870300BELMONT, PODIATRY X-RAY - REMEX, MODEL PD75K861328NEW BELMONT MODEL, MC-5 DENTAL, INTRAORAL X-RAY

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Related Devices (Code: EIA)

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.

K251544Dental Unit (MP2000-550LED-2.0, LP2100-550LED-2.0)Lakong Medical Devices Co., Ltd.K251626Midmark Dental Delivery SystemMidmark CorporationK251491K5 Cart, K5 Mount, K5 SwingOsstem Implant Company., Ltd. Chair BusinessK243130Integral Dental UnitGuangdong Yadeng Medical Apparatus Co., Ltd.,K242611Integral Dental UnitsMipont Medical Equipment Co., Ltd.K250473Dental Delivery System Series 5 and Dental Delivery System Series 5 PlusDci International, LLC

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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