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FDA 510(k)

MASTER-VU

K-Number: K073196 · 2007-12-19

ApplicantSonomed, Inc.
Decision Date2007-12-19
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MASTER-VU is the device name listed in this FDA 510(k) record. The listed applicant is Sonomed, Inc.. It received FDA 510(k) clearance on 2007-12-19 under 510(k) number K073196. The device is classified under product code IYO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MASTER-VU?

MASTER-VU is a medical device that received FDA 510(k) clearance on 2007-12-19. The listed applicant is Sonomed, Inc.. The 510(k) number is K073196.

When did MASTER-VU receive FDA 510(k) clearance?

MASTER-VU received FDA 510(k) clearance on 2007-12-19, under 510(k) number K073196.

Who is the listed applicant for MASTER-VU?

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

What is the FDA product code for MASTER-VU?

The FDA product code for MASTER-VU is IYO.

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Other records listing Sonomed, 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.

K171098AXIS Image Management SystemK100252MASTER-VU A-SCAN, MV4500K092637PACSCAN PLUS, MODELS 300P AND 300APK060626VUMAXK040668E-Z SCAN AB5500+K924311SONOMED 4000P ULTRASONIC PACHYMETER

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Related Devices (Code: IYO)

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.

K260313MD-6000S Bladder ScannerMEDA Co., Ltd.K253452Accuro 3SRivanna Medical, Inc.K260190ARTHURROPCA ApSK252237EdgeFlow UW20Edgecare, Inc.K254021Accuro XVRivanna Medical, Inc.K253898QT Scanner 2000 Model AQT Imaging Holdings, 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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