FDA 510(k)

C.C. LIFE 21

K-Number: K213295 · 2022-11-17

Decision Date2022-11-17

Product CodePBX

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

C.C. LIFE 21 is the device name listed in this FDA 510(k) record. The listed applicant is 21 Equipment S.R.L.. It received FDA 510(k) clearance on 2022-11-17 under 510(k) 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. The listed applicant is 21 Equipment S.R.L.. The 510(k) number is K213295.

When did C.C. LIFE 21 receive FDA 510(k) clearance?

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

Who is the listed applicant for C.C. LIFE 21?

The FDA 510(k) record lists 21 Equipment S.R.L. as the applicant. This does not by itself establish the device manufacturer.

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

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

Other records listing 21 Equipment S.R.L. 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.

K230459C.C. Life 21

Related Devices (Code: PBX)

K253480Capenergy C Equipments RF C200 and C400 DrakarianCapenergy Medical S.L.K260647SPECCHIOEl.En S.P.A.K253261Apollo Quattro (APQ-10M)Weero Co., Ltd.K252888NeoSculpt PlusS&M Medical Co., Ltd.K250734OptiLUV DevicePollogen, Ltd.K250916WinForth (LM-E470KA)Shenzhen Leaflife Technology Co., Ltd.

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.