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FDA 510(k)

DOPPLER NEEDLE AND FLOW MONITOR

K-Number: K903625 · 1990-11-07

ApplicantPeripheral Systems Group
Decision Date1990-11-07
Product CodeDPW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

DOPPLER NEEDLE AND FLOW MONITOR is the device name listed in this FDA 510(k) record. The listed applicant is Peripheral Systems Group. It received FDA 510(k) clearance on 1990-11-07 under 510(k) number K903625. 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 DOPPLER NEEDLE AND FLOW MONITOR?

DOPPLER NEEDLE AND FLOW MONITOR is a medical device that received FDA 510(k) clearance on 1990-11-07. The listed applicant is Peripheral Systems Group. The 510(k) number is K903625.

When did DOPPLER NEEDLE AND FLOW MONITOR receive FDA 510(k) clearance?

DOPPLER NEEDLE AND FLOW MONITOR received FDA 510(k) clearance on 1990-11-07, under 510(k) number K903625.

Who is the listed applicant for DOPPLER NEEDLE AND FLOW MONITOR?

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

What is the FDA product code for DOPPLER NEEDLE AND FLOW MONITOR?

The FDA product code for DOPPLER NEEDLE AND FLOW MONITOR is DPW.

Related Clinical Trials

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Other records listing Peripheral Systems Group as applicant

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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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