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FDA 510(k)

MODEL AMI1200 C-ARM

K-Number: K022911 · 2002-12-02

ApplicantIntegrity Practice Management, Inc.
Decision Date2002-12-02
Product CodeJAA
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MODEL AMI1200 C-ARM is the device name listed in this FDA 510(k) record. The listed applicant is Integrity Practice Management, Inc.. It received FDA 510(k) clearance on 2002-12-02 under 510(k) number K022911. The device is classified under product code JAA. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL AMI1200 C-ARM?

MODEL AMI1200 C-ARM is a medical device that received FDA 510(k) clearance on 2002-12-02. The listed applicant is Integrity Practice Management, Inc.. The 510(k) number is K022911.

When did MODEL AMI1200 C-ARM receive FDA 510(k) clearance?

MODEL AMI1200 C-ARM received FDA 510(k) clearance on 2002-12-02, under 510(k) number K022911.

Who is the listed applicant for MODEL AMI1200 C-ARM?

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

What is the FDA product code for MODEL AMI1200 C-ARM?

The FDA product code for MODEL AMI1200 C-ARM is JAA.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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