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FDA 510(k)

COLOR VELOCITY IMAGING (CVI) OPTION FOR PLATINUM

K-Number: K902926 · 1990-11-26

ApplicantPhilips Medical Systems North America, Inc.
Decision Date1990-11-26
Product CodeITX
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

COLOR VELOCITY IMAGING (CVI) OPTION FOR PLATINUM is the device name listed in this FDA 510(k) record. The listed applicant is Philips Medical Systems North America, Inc.. It received FDA 510(k) clearance on 1990-11-26 under 510(k) number K902926. The device is classified under product code ITX. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COLOR VELOCITY IMAGING (CVI) OPTION FOR PLATINUM?

COLOR VELOCITY IMAGING (CVI) OPTION FOR PLATINUM is a medical device that received FDA 510(k) clearance on 1990-11-26. The listed applicant is Philips Medical Systems North America, Inc.. The 510(k) number is K902926.

When did COLOR VELOCITY IMAGING (CVI) OPTION FOR PLATINUM receive FDA 510(k) clearance?

COLOR VELOCITY IMAGING (CVI) OPTION FOR PLATINUM received FDA 510(k) clearance on 1990-11-26, under 510(k) number K902926.

Who is the listed applicant for COLOR VELOCITY IMAGING (CVI) OPTION FOR PLATINUM?

The FDA 510(k) record lists Philips Medical Systems North America, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for COLOR VELOCITY IMAGING (CVI) OPTION FOR PLATINUM?

The FDA product code for COLOR VELOCITY IMAGING (CVI) OPTION FOR PLATINUM is ITX.

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Other records listing Philips Medical Systems North America, 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.

K102005ALLURA XPER OR TABLE SERIESK062233HEARTSTART MRX MONITOR/DEFIBRILLATORK062283THE PHILIPS MP20, MP30, MP40, MP50, MP60, MP70, MP80, MP90 INTELLIVUE PATIENT MONITORSK061052THE PHILIPS INTELLIVUE PATIENT MONITORS, MODELS MP20,MP30,MP40,MP50,MP60,MP70,MP80,MP90K050151MULTIDIAGNOST ELEVAK042867PHILIPS ORTHOPAEDIC APPLICATIONS

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Related Devices (Code: ITX)

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.

K260114Align® Cover and Pad Guidance ToolCIVCO Medical Instruments Co., Inc.K261170BA-004CCFujifilm CorporationK254143EM-TECH Passive Ultrasound Probe StrapEM-TECH Solutions, Inc.K260161SmartGuide Disposable Guides and GridsUC-CARE , Ltd.K262474ND Needle Guidance SystemAccurate Access, LLCK261014Accuro® 3S Needle Guide KitRivanna 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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