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FDA 510(k)

ECHO. AKHO

K-Number: K951976 · 1996-07-26

ApplicantAlliance Medical, Inc.
Decision Date1996-07-26
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ECHO. AKHO is the device name listed in this FDA 510(k) record. The listed applicant is Alliance Medical, Inc.. It received FDA 510(k) clearance on 1996-07-26 under 510(k) number K951976. 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 ECHO. AKHO?

ECHO. AKHO is a medical device that received FDA 510(k) clearance on 1996-07-26. The listed applicant is Alliance Medical, Inc.. The 510(k) number is K951976.

When did ECHO. AKHO receive FDA 510(k) clearance?

ECHO. AKHO received FDA 510(k) clearance on 1996-07-26, under 510(k) number K951976.

Who is the listed applicant for ECHO. AKHO?

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

What is the FDA product code for ECHO. AKHO?

The FDA product code for ECHO. AKHO is IYO.

Other records listing Alliance Medical, 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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