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)

VANTAGE MODEL V5000, V5100, V5000C, V5100C

K-Number: K122643 · 2013-01-07

ApplicantMidmark Corp.
Decision Date2013-01-07
Product CodeMUH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

VANTAGE MODEL V5000, V5100, V5000C, V5100C is the device name listed in this FDA 510(k) record. The listed applicant is Midmark Corp.. It received FDA 510(k) clearance on 2013-01-07 under 510(k) number K122643. The device is classified under product code MUH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VANTAGE MODEL V5000, V5100, V5000C, V5100C?

VANTAGE MODEL V5000, V5100, V5000C, V5100C is a medical device that received FDA 510(k) clearance on 2013-01-07. The listed applicant is Midmark Corp.. The 510(k) number is K122643.

When did VANTAGE MODEL V5000, V5100, V5000C, V5100C receive FDA 510(k) clearance?

VANTAGE MODEL V5000, V5100, V5000C, V5100C received FDA 510(k) clearance on 2013-01-07, under 510(k) number K122643.

Who is the listed applicant for VANTAGE MODEL V5000, V5100, V5000C, V5100C?

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

What is the FDA product code for VANTAGE MODEL V5000, V5100, V5000C, V5100C?

The FDA product code for VANTAGE MODEL V5000, V5100, V5000C, V5100C is MUH.

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 Midmark 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.

K112380CLEARVISIONK090670MIDMARK M3 ULTRAFAST AUTOMATIC STERILIZERK023348MIDMARK M9 ULTRACLAVE STEAM STERILIZERK003090MIDMARK PROCENTER INSTRUMENT DELIVERY SYSTEMK992744MIDMARK M4*9 EASYCLAVE STEAM STERILIZERK990189MODIFICATION OF: MIDMARK M-11 ULTRACLAVE STEAM STERILIZER

View all 31 devices →

Related Devices (Code: MUH)

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.

K251793SOTA Cloud Smart Sensor (1.5)Sota Cloud Corp.K252570EzSensor HD, EzSensor UHDQpix Solutions, Inc.K250687Cocoon Solo (DX-7020s)Dexcowin Global, Inc.K251206Digital X-Ray DentiMax Pro Imaging SystemDentimax, Inc.K240040VistaPano S Ceph 2.0 (VistaPano S Ceph); VistaPano S 2.0 (VistaPano S); ProVecta S-Pan Ceph 2.0 (ProVecta S-Pan Ceph); ProVecta S-Pan 2.0 (ProVecta S-Pan)VATECH Co., Ltd.K242778X Sensor (Model: IOS-A15IF, HDI-15DGF)Qpix Solutions, Inc.

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.

↑