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FDA 510(k)

MOORVMS-PRES PRESSURE CUFF CONTROLLER

K-Number: K102433 · 2010-11-18

ApplicantMoor Instruments, Ltd.
Decision Date2010-11-18
Product CodeDPW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MOORVMS-PRES PRESSURE CUFF CONTROLLER is the device name listed in this FDA 510(k) record. The listed applicant is Moor Instruments, Ltd.. It received FDA 510(k) clearance on 2010-11-18 under 510(k) number K102433. 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 MOORVMS-PRES PRESSURE CUFF CONTROLLER?

MOORVMS-PRES PRESSURE CUFF CONTROLLER is a medical device that received FDA 510(k) clearance on 2010-11-18. The listed applicant is Moor Instruments, Ltd.. The 510(k) number is K102433.

When did MOORVMS-PRES PRESSURE CUFF CONTROLLER receive FDA 510(k) clearance?

MOORVMS-PRES PRESSURE CUFF CONTROLLER received FDA 510(k) clearance on 2010-11-18, under 510(k) number K102433.

Who is the listed applicant for MOORVMS-PRES PRESSURE CUFF CONTROLLER?

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

What is the FDA product code for MOORVMS-PRES PRESSURE CUFF CONTROLLER?

The FDA product code for MOORVMS-PRES PRESSURE CUFF CONTROLLER is DPW.

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Other records listing Moor Instruments, Ltd. as applicant

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K152749moorLDI2-IR Infrared laser Doppler imager, moorLDI2-HIR High Resolution Infrared laser Doppler imager, moorLDI2-VR Visible Red laser Doppler imagerK122943MOORFLPI-2 FULL-FIELD LASER PERFUSION IMAGERK112826NOORVMS-OXY TISSUE OXYGEN AND TEMPERTURE MONITORK083082MOORVMS-LDF1 AND MOORVMS-LDF2 LASER DOPPLER PERFUSION AND TEMPERATURE MONITORSK060976MOORLD12-B1 LASER DOPPLER BURNS IMAGERK063586MOORFLPI FULL-FIELD LASER PERFUSION IMAGER

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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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