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FDA 510(k)

Deka Tiac 1

K-Number: K183371 · 2019-12-03

ApplicantEl..En. Electroic Engineering Spa
Decision Date2019-12-03
Product CodePBX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Deka Tiac 1 is a medical device manufactured by El..En. Electroic Engineering Spa. It received FDA 510(k) clearance on 2019-12-03 under approval number K183371. The device is classified under product code PBX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Deka Tiac 1?

Deka Tiac 1 is a medical device that received FDA 510(k) clearance on 2019-12-03. It is manufactured by El..En. Electroic Engineering Spa. The 510(k) number is K183371.

When was Deka Tiac 1 approved by the FDA?

Deka Tiac 1 received FDA 510(k) clearance on 2019-12-03, under approval number K183371.

What company makes Deka Tiac 1?

Deka Tiac 1 is manufactured by El..En. Electroic Engineering Spa.

What is the FDA product code for Deka Tiac 1?

The FDA product code for Deka Tiac 1 is PBX.

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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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