FDA 510(k)

AIM

K-Number: K121479 · 2012-09-13

Decision Date2012-09-13

Product CodeIYO

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

AIM is the device name listed in this FDA 510(k) record. The listed applicant is Inneroptic Technology, Inc.. It received FDA 510(k) clearance on 2012-09-13 under 510(k) number K121479. 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 AIM?

AIM is a medical device that received FDA 510(k) clearance on 2012-09-13. The listed applicant is Inneroptic Technology, Inc.. The 510(k) number is K121479.

When did AIM receive FDA 510(k) clearance?

AIM received FDA 510(k) clearance on 2012-09-13, under 510(k) number K121479.

Who is the listed applicant for AIM?

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

What is the FDA product code for AIM?

The FDA product code for AIM is IYO.

Other records listing Inneroptic Technology, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K083728INVISION SYSTEM

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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.