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FDA 510(k)

MICRON, MICROVASCULAR DOPPLER

K-Number: K860651 · 1986-07-18

ApplicantDiagnostic Electronics Corp.
Decision Date1986-07-18
Product CodeDPW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MICRON, MICROVASCULAR DOPPLER is the device name listed in this FDA 510(k) record. The listed applicant is Diagnostic Electronics Corp.. It received FDA 510(k) clearance on 1986-07-18 under 510(k) number K860651. 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 MICRON, MICROVASCULAR DOPPLER?

MICRON, MICROVASCULAR DOPPLER is a medical device that received FDA 510(k) clearance on 1986-07-18. The listed applicant is Diagnostic Electronics Corp.. The 510(k) number is K860651.

When did MICRON, MICROVASCULAR DOPPLER receive FDA 510(k) clearance?

MICRON, MICROVASCULAR DOPPLER received FDA 510(k) clearance on 1986-07-18, under 510(k) number K860651.

Who is the listed applicant for MICRON, MICROVASCULAR DOPPLER?

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

What is the FDA product code for MICRON, MICROVASCULAR DOPPLER?

The FDA product code for MICRON, MICROVASCULAR 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.

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Other records listing Diagnostic Electronics Corp. 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.

K861023DOPPLEX, PULSED/CONTINUOUS WAVE DOPPOLERK830628REAL-TIME SPECTRUM ANALYZER

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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