Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

OHMNISCAN NG

K-Number: K073334 · 2008-08-22

ApplicantChristine Valmy, Inc.
Decision Date2008-08-22
Product CodeMNW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

OHMNISCAN NG is the device name listed in this FDA 510(k) record. The listed applicant is Christine Valmy, Inc.. It received FDA 510(k) clearance on 2008-08-22 under 510(k) number K073334. The device is classified under product code MNW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OHMNISCAN NG?

OHMNISCAN NG is a medical device that received FDA 510(k) clearance on 2008-08-22. The listed applicant is Christine Valmy, Inc.. The 510(k) number is K073334.

When did OHMNISCAN NG receive FDA 510(k) clearance?

OHMNISCAN NG received FDA 510(k) clearance on 2008-08-22, under 510(k) number K073334.

Who is the listed applicant for OHMNISCAN NG?

The FDA 510(k) record lists Christine Valmy, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for OHMNISCAN NG?

The FDA product code for OHMNISCAN NG is MNW.

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

Related Devices (Code: MNW)

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.

K231116Multi-parameter detectorZhongshan Jinli Electronic Weighing Equipment Co., Ltd.K130856BIA / VITALITY ANALYZERIpgdx, LLCK130777INBODYBiospace Corporation LimitedK130952PRECISION ONE LIFECARE; DETECTO; DETECTOPrecision One Lifecare, Ltd.K131394TRANSTEK GLASS BODY FAT ANALYZERGuangdong Transtek Medical Electronics Co., Ltd.K130311TRANSTEK BODY FAT ANALYZERGuangdong Transtek Medical Electronics 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.

↑