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FDA 510(k)

C.C. LIFE 21

K-Number: K213295 · 2022-11-17

Applicant21 Equipment S.R.L.
Decision Date2022-11-17
Product CodePBX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

C.C. LIFE 21 is a medical device manufactured by 21 Equipment S.R.L.. It received FDA 510(k) clearance on 2022-11-17 under approval number K213295. 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 C.C. LIFE 21?

C.C. LIFE 21 is a medical device that received FDA 510(k) clearance on 2022-11-17. It is manufactured by 21 Equipment S.R.L.. The 510(k) number is K213295.

When was C.C. LIFE 21 approved by the FDA?

C.C. LIFE 21 received FDA 510(k) clearance on 2022-11-17, under approval number K213295.

What company makes C.C. LIFE 21?

C.C. LIFE 21 is manufactured by 21 Equipment S.R.L..

What is the FDA product code for C.C. LIFE 21?

The FDA product code for C.C. LIFE 21 is PBX.

Other Devices by 21 Equipment S.R.L.

K230459C.C. Life 21

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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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