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FDA 510(k)

MODULAT DENTAL SYSTEMS

K-Number: K781882 · 1978-12-28

ApplicantVacudent Sales Corp.
Decision Date1978-12-28
Product CodeEIA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MODULAT DENTAL SYSTEMS is the device name listed in this FDA 510(k) record. The listed applicant is Vacudent Sales Corp.. It received FDA 510(k) clearance on 1978-12-28 under 510(k) number K781882. 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 MODULAT DENTAL SYSTEMS?

MODULAT DENTAL SYSTEMS is a medical device that received FDA 510(k) clearance on 1978-12-28. The listed applicant is Vacudent Sales Corp.. The 510(k) number is K781882.

When did MODULAT DENTAL SYSTEMS receive FDA 510(k) clearance?

MODULAT DENTAL SYSTEMS received FDA 510(k) clearance on 1978-12-28, under 510(k) number K781882.

Who is the listed applicant for MODULAT DENTAL SYSTEMS?

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

What is the FDA product code for MODULAT DENTAL SYSTEMS?

The FDA product code for MODULAT DENTAL SYSTEMS is EIA.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Vacudent Sales 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.

K800574VACUDENT LUMIX 65K800575VACUDENT LUMIX 70K800520DENTAL STOOLS, #'S P2212, P1121, ETC.

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

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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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