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FDA 510(k)

FEATHERLITE AQUA TOCODYNAMOMETER

K-Number: K061044 · 2006-07-12

ApplicantVentrex, Inc.
Decision Date2006-07-12
Product CodeHFM
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

FEATHERLITE AQUA TOCODYNAMOMETER is the device name listed in this FDA 510(k) record. The listed applicant is Ventrex, Inc.. It received FDA 510(k) clearance on 2006-07-12 under 510(k) number K061044. The device is classified under product code HFM. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FEATHERLITE AQUA TOCODYNAMOMETER?

FEATHERLITE AQUA TOCODYNAMOMETER is a medical device that received FDA 510(k) clearance on 2006-07-12. The listed applicant is Ventrex, Inc.. The 510(k) number is K061044.

When did FEATHERLITE AQUA TOCODYNAMOMETER receive FDA 510(k) clearance?

FEATHERLITE AQUA TOCODYNAMOMETER received FDA 510(k) clearance on 2006-07-12, under 510(k) number K061044.

Who is the listed applicant for FEATHERLITE AQUA TOCODYNAMOMETER?

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

What is the FDA product code for FEATHERLITE AQUA TOCODYNAMOMETER?

The FDA product code for FEATHERLITE AQUA TOCODYNAMOMETER is HFM.

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 Ventrex, Inc. 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.

K013477TOCO LITE, MODEL TD-01K964821COVEROX SHEATH MODELS NUMBER PS65, PS67, EPS65 AND EPS67K925044VENTREX ALLERGEN DISCK924119VENTREX ALLERGEN DISC

Related Devices (Code: HFM)

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.

K040392TRANSDUCERS FOR ULTRASOUND AND TOCODYNAMOMETER FETAL MONITORINGAmerican I.V. Products, Inc.K013477TOCO LITE, MODEL TD-01Ventrex, Inc.K994353SECURELINE DISPOSABLE FETAL MONITORING STRAPS #3860 AND #3565Precision Dynamics Corp.K992811TRANSDUCERS FOR ULTRASOUND AND TOCODYNAMOMETER FETAL MONITORINGEpic Medical Equipment Services, Inc.K954847DISCO UTERINE CONTRACTION TRANSDUCER & ACCESSORIESOcg Systems, Inc.K952579TOCO TRANSDUCERScientific Device Manufacturer, 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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