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FDA 510(k)

AROMACRYL

K-Number: K021121 · 2002-05-28

ApplicantAromacryl, LLC
Decision Date2002-05-28
Product CodeEBI
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

AROMACRYL is the device name listed in this FDA 510(k) record. The listed applicant is Aromacryl, LLC. It received FDA 510(k) clearance on 2002-05-28 under 510(k) number K021121. The device is classified under product code EBI. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AROMACRYL?

AROMACRYL is a medical device that received FDA 510(k) clearance on 2002-05-28. The listed applicant is Aromacryl, LLC. The 510(k) number is K021121.

When did AROMACRYL receive FDA 510(k) clearance?

AROMACRYL received FDA 510(k) clearance on 2002-05-28, under 510(k) number K021121.

Who is the listed applicant for AROMACRYL?

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

What is the FDA product code for AROMACRYL?

The FDA product code for AROMACRYL is EBI.

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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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