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FDA 510(k)

ARI COLD SPRAY

K-Number: K033720 · 2005-06-10

ApplicantAri
Decision Date2005-06-10
Product CodeMLY
DecisionSubstantially Equivalent

Device Summary

ARI COLD SPRAY is the device name listed in this FDA 510(k) record. The listed applicant is Ari. It received FDA 510(k) clearance on 2005-06-10 under 510(k) number K033720. The device is classified under product code MLY. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARI COLD SPRAY?

ARI COLD SPRAY is a medical device that received FDA 510(k) clearance on 2005-06-10. The listed applicant is Ari. The 510(k) number is K033720.

When did ARI COLD SPRAY receive FDA 510(k) clearance?

ARI COLD SPRAY received FDA 510(k) clearance on 2005-06-10, under 510(k) number K033720.

Who is the listed applicant for ARI COLD SPRAY?

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

What is the FDA product code for ARI COLD SPRAY?

The FDA product code for ARI COLD SPRAY is MLY.

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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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