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FDA 510(k)

MASTER-VU A-SCAN, MV4500

K-Number: K100252 · 2010-04-09

ApplicantSonomed, Inc.
Decision Date2010-04-09
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MASTER-VU A-SCAN, MV4500 is the device name listed in this FDA 510(k) record. The listed applicant is Sonomed, Inc.. It received FDA 510(k) clearance on 2010-04-09 under 510(k) number K100252. 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 A-SCAN, MV4500?

MASTER-VU A-SCAN, MV4500 is a medical device that received FDA 510(k) clearance on 2010-04-09. The listed applicant is Sonomed, Inc.. The 510(k) number is K100252.

When did MASTER-VU A-SCAN, MV4500 receive FDA 510(k) clearance?

MASTER-VU A-SCAN, MV4500 received FDA 510(k) clearance on 2010-04-09, under 510(k) number K100252.

Who is the listed applicant for MASTER-VU A-SCAN, MV4500?

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 A-SCAN, MV4500?

The FDA product code for MASTER-VU A-SCAN, MV4500 is IYO.

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Other records listing Sonomed, Inc. as applicant

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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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