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FDA 510(k)

S dispensing line

K-Number: K192770 · 2020-12-17

ApplicantAea Srl
Decision Date2020-12-17
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

S dispensing line is the device name listed in this FDA 510(k) record. The listed applicant is Aea Srl. It received FDA 510(k) clearance on 2020-12-17 under 510(k) number K192770. The device is classified under product code FMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the S dispensing line?

S dispensing line is a medical device that received FDA 510(k) clearance on 2020-12-17. The listed applicant is Aea Srl. The 510(k) number is K192770.

When did S dispensing line receive FDA 510(k) clearance?

S dispensing line received FDA 510(k) clearance on 2020-12-17, under 510(k) number K192770.

Who is the listed applicant for S dispensing line?

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

What is the FDA product code for S dispensing line?

The FDA product code for S dispensing line is FMF.

Other records listing Aea Srl 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.

Related Devices (Code: FMF)

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.

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.