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FDA 510(k)

ARCO FP

K-Number: K182086 · 2019-08-20

ApplicantA.T.S. Applicazione Tecnologie Speciali S.R.L.
Decision Date2019-08-20
Product CodeOWB
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ARCO FP is a medical device manufactured by A.T.S. Applicazione Tecnologie Speciali S.R.L.. It received FDA 510(k) clearance on 2019-08-20 under approval number K182086. The device is classified under product code OWB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARCO FP?

ARCO FP is a medical device that received FDA 510(k) clearance on 2019-08-20. It is manufactured by A.T.S. Applicazione Tecnologie Speciali S.R.L.. The 510(k) number is K182086.

When was ARCO FP approved by the FDA?

ARCO FP received FDA 510(k) clearance on 2019-08-20, under approval number K182086.

What company makes ARCO FP?

ARCO FP is manufactured by A.T.S. Applicazione Tecnologie Speciali S.R.L..

What is the FDA product code for ARCO FP?

The FDA product code for ARCO FP is OWB.

Other Devices by A.T.S. Applicazione Tecnologie Speciali S.R.L.

K211777ARCO FP-S K211542PRIMO S K250282Persona C HR

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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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