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FDA 510(k)

CONTINUOUS WAVE DOPPLER

K-Number: K760751 · 1976-10-13

ApplicantMedsonics
Decision Date1976-10-13
Product CodeDPW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CONTINUOUS WAVE DOPPLER is the device name listed in this FDA 510(k) record. The listed applicant is Medsonics. It received FDA 510(k) clearance on 1976-10-13 under 510(k) number K760751. The device is classified under product code DPW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CONTINUOUS WAVE DOPPLER?

CONTINUOUS WAVE DOPPLER is a medical device that received FDA 510(k) clearance on 1976-10-13. The listed applicant is Medsonics. The 510(k) number is K760751.

When did CONTINUOUS WAVE DOPPLER receive FDA 510(k) clearance?

CONTINUOUS WAVE DOPPLER received FDA 510(k) clearance on 1976-10-13, under 510(k) number K760751.

Who is the listed applicant for CONTINUOUS WAVE DOPPLER?

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

What is the FDA product code for CONTINUOUS WAVE DOPPLER?

The FDA product code for CONTINUOUS WAVE DOPPLER is DPW.

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 Medsonics 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.

K770904PROBE, BLOOD FLOW DETECTOR PLUG-INK770332AMPLIFIER, PHOTOPULSE, MODEL PA13K760728CONTINUOUS WAVE DOPPLER ULTRASOUND

Related Devices (Code: DPW)

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.

K260700BlueDop Vascular ExpertBlueDop Medical, Ltd.K252810FloPatch FP120Flosonics MedicalK251904VascuChek Kit, VascuChek Transceiver, VascuChek Clinical Probe, VascuChek Speaker Dock (VC-KIT-02, VC-TRX-02, VC-CP-01, VC-SD-01); VascuChek Kit, VascuChek Transceiver, VascuChek Surgical Probe, VascuChek Speaker Dock (VC-KIT-02, VC-TRX-02, VC-SP-01, VC-SD-01)Remington Medical, Inc.K251114FloPatch FP120Flosonics MedicalK243852Elfor-LElfi-Tech , Ltd.K241583VascuChek Kit, VascuChek Transceiver, VascuChek Clinical Probe, VascuChek Charger (VC-KIT-01, VC-TRX-01, VC-CP-01, VC-CH-01); VascuChek Kit, VascuChek Transceiver, VascuChek Surgical Probe, VascuChek Charger (VC-KIT-01, VC-TRX-01, VC-SP-01, VC-CH-01)Remington Medical, 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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