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FDA 510(k)

VTI INTRAOPERATIVE DOPPLER SYSTEMS

K-Number: K082870 · 2008-10-28

ApplicantVascular Technology Incorporated
Decision Date2008-10-28
Product CodeDPW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

VTI INTRAOPERATIVE DOPPLER SYSTEMS is the device name listed in this FDA 510(k) record. The listed applicant is Vascular Technology Incorporated. It received FDA 510(k) clearance on 2008-10-28 under 510(k) number K082870. 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 VTI INTRAOPERATIVE DOPPLER SYSTEMS?

VTI INTRAOPERATIVE DOPPLER SYSTEMS is a medical device that received FDA 510(k) clearance on 2008-10-28. The listed applicant is Vascular Technology Incorporated. The 510(k) number is K082870.

When did VTI INTRAOPERATIVE DOPPLER SYSTEMS receive FDA 510(k) clearance?

VTI INTRAOPERATIVE DOPPLER SYSTEMS received FDA 510(k) clearance on 2008-10-28, under 510(k) number K082870.

Who is the listed applicant for VTI INTRAOPERATIVE DOPPLER SYSTEMS?

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

What is the FDA product code for VTI INTRAOPERATIVE DOPPLER SYSTEMS?

The FDA product code for VTI INTRAOPERATIVE DOPPLER SYSTEMS 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.

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Other records listing Vascular Technology Incorporated 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.

K031091VTI 20 MHZ GATED DOPPLERK002990VTI ADULT DISPOSABLE SKULL PIN, MODEL 22000; VTI SKULL SCREW, MODEL 22001K944764VTI DISPOSABLE PRESSURE DISPLAY SETK922738VTI OXYGEN ANALYZERK890058VASCULAR TECHNOLOGY UNIOX OXYGEN ALARMK883960GIPHY MONITOR

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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

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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