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FDA 510(k)

MILLAR PULSED DOPPLER VELOCIMETER

K-Number: K860766 · 1986-07-29

ApplicantMillar Instruments, Inc.
Decision Date1986-07-29
Product CodeDPW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MILLAR PULSED DOPPLER VELOCIMETER is the device name listed in this FDA 510(k) record. The listed applicant is Millar Instruments, Inc.. It received FDA 510(k) clearance on 1986-07-29 under 510(k) number K860766. 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 MILLAR PULSED DOPPLER VELOCIMETER?

MILLAR PULSED DOPPLER VELOCIMETER is a medical device that received FDA 510(k) clearance on 1986-07-29. The listed applicant is Millar Instruments, Inc.. The 510(k) number is K860766.

When did MILLAR PULSED DOPPLER VELOCIMETER receive FDA 510(k) clearance?

MILLAR PULSED DOPPLER VELOCIMETER received FDA 510(k) clearance on 1986-07-29, under 510(k) number K860766.

Who is the listed applicant for MILLAR PULSED DOPPLER VELOCIMETER?

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

What is the FDA product code for MILLAR PULSED DOPPLER VELOCIMETER?

The FDA product code for MILLAR PULSED DOPPLER VELOCIMETER is DPW.

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Other records listing Millar Instruments, 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.

K112323CARDIA-CATHK093111MIKRO-CATH, MODEL 825-0101K013205MILLAR PRESSURE CONTROL UNIT MODEL PCU-2000K993694MIKRO-TIP ANGIOGRAPHIC CATHETERK952773MIKRO-TIP ANGIOGRAPHIC CATHETERK935166FLOW DIRECTED MIKRO-TIP PRESSURE TRANSDUCER

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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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