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FDA 510(k)

VITAJET

K-Number: K962625 · 1996-12-10

ApplicantVitajet Corp.
Decision Date1996-12-10
Product CodeKZE
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

VITAJET is the device name listed in this FDA 510(k) record. The listed applicant is Vitajet Corp.. It received FDA 510(k) clearance on 1996-12-10 under 510(k) number K962625. The device is classified under product code KZE. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VITAJET?

VITAJET is a medical device that received FDA 510(k) clearance on 1996-12-10. The listed applicant is Vitajet Corp.. The 510(k) number is K962625.

When did VITAJET receive FDA 510(k) clearance?

VITAJET received FDA 510(k) clearance on 1996-12-10, under 510(k) number K962625.

Who is the listed applicant for VITAJET?

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

What is the FDA product code for VITAJET?

The FDA product code for VITAJET is KZE.

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 Vitajet 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.

K945548MEDIVAXK924447VITAPEN

Related Devices (Code: KZE)

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.

K121270BIOJECT NEEDLE-FREE INJECTION MANAGEMENT SYSTEMBioject Medical Technologies, Inc.K111517PHARMAJET STRATIS 0.5 ML NEEDLE-FREE INJECTION SYSTEM MODEL 501-01, STRATIS INJECTOR CATALOG 501-10, STRATIS RESET STATIPharmajet, Inc.K110456PHARMAJET 0.1 ML INTRADERMAL NEEDLE-FREE INJECTION SYSTEMPharmajet, Inc.K090959LECTRAJET NEEDLE-FREE INJECTION SYSTEM, MODEL: M3 RAD'Antonio Consultants International, Inc. (Dci)K090003ZETAJETBioject, Inc.K081532PHARMAJET NEEDLE-FREE INJECTION SYSTEMPharmajet, Inc.

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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