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FDA 510(k)

ELECTRONIC GRAVITY 300VC

K-Number: K833953 · 1983-12-29

ApplicantIvent Corp.
Decision Date1983-12-29
Product CodeLDR
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ELECTRONIC GRAVITY 300VC is the device name listed in this FDA 510(k) record. The listed applicant is Ivent Corp.. It received FDA 510(k) clearance on 1983-12-29 under 510(k) number K833953. The device is classified under product code LDR. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ELECTRONIC GRAVITY 300VC?

ELECTRONIC GRAVITY 300VC is a medical device that received FDA 510(k) clearance on 1983-12-29. The listed applicant is Ivent Corp.. The 510(k) number is K833953.

When did ELECTRONIC GRAVITY 300VC receive FDA 510(k) clearance?

ELECTRONIC GRAVITY 300VC received FDA 510(k) clearance on 1983-12-29, under 510(k) number K833953.

Who is the listed applicant for ELECTRONIC GRAVITY 300VC?

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

What is the FDA product code for ELECTRONIC GRAVITY 300VC?

The FDA product code for ELECTRONIC GRAVITY 300VC is LDR.

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 Ivent 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.

K852259IVENT INTRAVENOUS ADMINSTRATION SETK842210IVENT 302VC DUAL CONTROLLER

Related Devices (Code: LDR)

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.

K242693DEKA Infusion System, DEKA Administration SetDeka Research and Development CorporationK232316DEKA Infusion System, DEKA Administration SetDeka Research and DevelopmentK153760Volumetric Infusion ControllerDEKA Research & DevelopmentK963136PACER MODEL 100 INFUSION CONTROLLERHealth Watch, Inc.K971826ALEXANDER MANUFACTURING CO. RECHARGEABLE BATTERY PART NUMBER M12/500Alexander Mfg. Co.K971865ALEXANDER MANUFACTURING CO. RECHARGEABLE BATTERY PART NUMBER M12/500-3PAlexander Mfg. Co.

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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