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FDA 510(k)

VUMAX

K-Number: K060626 · 2006-04-11

ApplicantSonomed, Inc.
Decision Date2006-04-11
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

VUMAX is the device name listed in this FDA 510(k) record. The listed applicant is Sonomed, Inc.. It received FDA 510(k) clearance on 2006-04-11 under 510(k) number K060626. 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 VUMAX?

VUMAX is a medical device that received FDA 510(k) clearance on 2006-04-11. The listed applicant is Sonomed, Inc.. The 510(k) number is K060626.

When did VUMAX receive FDA 510(k) clearance?

VUMAX received FDA 510(k) clearance on 2006-04-11, under 510(k) number K060626.

Who is the listed applicant for VUMAX?

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 VUMAX?

The FDA product code for VUMAX 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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