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FDA 510(k)

DOPPLEX, PULSED/CONTINUOUS WAVE DOPPOLER

K-Number: K861023 · 1986-11-17

ApplicantDiagnostic Electronics Corp.
Decision Date1986-11-17
Product CodeDPW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

DOPPLEX, PULSED/CONTINUOUS WAVE DOPPOLER 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 1986-11-17 under 510(k) number K861023. 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 DOPPLEX, PULSED/CONTINUOUS WAVE DOPPOLER?

DOPPLEX, PULSED/CONTINUOUS WAVE DOPPOLER is a medical device that received FDA 510(k) clearance on 1986-11-17. The listed applicant is Diagnostic Electronics Corp.. The 510(k) number is K861023.

When did DOPPLEX, PULSED/CONTINUOUS WAVE DOPPOLER receive FDA 510(k) clearance?

DOPPLEX, PULSED/CONTINUOUS WAVE DOPPOLER received FDA 510(k) clearance on 1986-11-17, under 510(k) number K861023.

Who is the listed applicant for DOPPLEX, PULSED/CONTINUOUS WAVE DOPPOLER?

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 DOPPLEX, PULSED/CONTINUOUS WAVE DOPPOLER?

The FDA product code for DOPPLEX, PULSED/CONTINUOUS WAVE DOPPOLER 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.

K860651MICRON, MICROVASCULAR DOPPLERK830628REAL-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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