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FDA 510(k)

VASOFLO-3 & EXTRAVASCULAR BLOOD FLOW PROBES

K-Number: K862720 · 1986-11-17

ApplicantSonicaid, Inc.
Decision Date1986-11-17
Product CodeDPW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

VASOFLO-3 & EXTRAVASCULAR BLOOD FLOW PROBES is the device name listed in this FDA 510(k) record. The listed applicant is Sonicaid, Inc.. It received FDA 510(k) clearance on 1986-11-17 under 510(k) number K862720. 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 VASOFLO-3 & EXTRAVASCULAR BLOOD FLOW PROBES?

VASOFLO-3 & EXTRAVASCULAR BLOOD FLOW PROBES is a medical device that received FDA 510(k) clearance on 1986-11-17. The listed applicant is Sonicaid, Inc.. The 510(k) number is K862720.

When did VASOFLO-3 & EXTRAVASCULAR BLOOD FLOW PROBES receive FDA 510(k) clearance?

VASOFLO-3 & EXTRAVASCULAR BLOOD FLOW PROBES received FDA 510(k) clearance on 1986-11-17, under 510(k) number K862720.

Who is the listed applicant for VASOFLO-3 & EXTRAVASCULAR BLOOD FLOW PROBES?

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

What is the FDA product code for VASOFLO-3 & EXTRAVASCULAR BLOOD FLOW PROBES?

The FDA product code for VASOFLO-3 & EXTRAVASCULAR BLOOD FLOW PROBES is DPW.

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Other records listing Sonicaid, 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.

K873673BV105 (&BV105R) VASCULAR FLOW DETECTOR W/OPTIONALK8720745 MHZ TRANSDUCERK863803VASOPULSE(TM)/MODEL 5000K861237VASOVIEW DUPLEX IMAGING SYSTEMK851102VASOSCREEN IMPEDANCE PLETHYSMOGRAPHK833902VASOSCAN

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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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