C.C. Life 21
K-Number: K230459 · 2023-10-19
Device Summary
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 2023-10-19. The listed applicant is 21 Equipment S.R.L.. The 510(k) number is K230459.
When did C.C. Life 21 receive FDA 510(k) clearance?
C.C. Life 21 received FDA 510(k) clearance on 2023-10-19, under 510(k) number K230459.
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 NFO.
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.
Related Devices (Code: NFO)
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.