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FDA 510(k)

Zone Specific AIM

K-Number: K220186 · 2022-05-13

ApplicantConmed Corporation
Decision Date2022-05-13
Product CodeGAT
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Zone Specific AIM is the device name listed in this FDA 510(k) record. The listed applicant is Conmed Corporation. It received FDA 510(k) clearance on 2022-05-13 under 510(k) number K220186. The device is classified under product code GAT. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Zone Specific AIM?

Zone Specific AIM is a medical device that received FDA 510(k) clearance on 2022-05-13. The listed applicant is Conmed Corporation. The 510(k) number is K220186.

When did Zone Specific AIM receive FDA 510(k) clearance?

Zone Specific AIM received FDA 510(k) clearance on 2022-05-13, under 510(k) number K220186.

Who is the listed applicant for Zone Specific AIM?

The FDA 510(k) record lists Conmed Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Zone Specific AIM?

The FDA product code for Zone Specific AIM is GAT.

Other records listing Conmed Corporation as applicant

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Related Devices (Code: GAT)

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.

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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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