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FDA 510(k)

AMIB7

K-Number: K990198 · 1999-06-29

ApplicantAlliance Medical, Inc.
Decision Date1999-06-29
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

AMIB7 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 1999-06-29 under 510(k) number K990198. 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 AMIB7?

AMIB7 is a medical device that received FDA 510(k) clearance on 1999-06-29. The listed applicant is Alliance Medical, Inc.. The 510(k) number is K990198.

When did AMIB7 receive FDA 510(k) clearance?

AMIB7 received FDA 510(k) clearance on 1999-06-29, under 510(k) number K990198.

Who is the listed applicant for AMIB7?

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 AMIB7?

The FDA product code for AMIB7 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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