ComASP Cefiderocol 0.008-128
K-Number: K230479 · 2023-05-18
Device Summary
Frequently Asked Questions
What is the ComASP Cefiderocol 0.008-128?
ComASP Cefiderocol 0.008-128 is a medical device that received FDA 510(k) clearance on 2023-05-18. The listed applicant is Liofilchem s.r.l.. The 510(k) number is K230479.
When did ComASP Cefiderocol 0.008-128 receive FDA 510(k) clearance?
ComASP Cefiderocol 0.008-128 received FDA 510(k) clearance on 2023-05-18, under 510(k) number K230479.
Who is the listed applicant for ComASP Cefiderocol 0.008-128?
The FDA 510(k) record lists Liofilchem s.r.l. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ComASP Cefiderocol 0.008-128?
The FDA product code for ComASP Cefiderocol 0.008-128 is JWY.
Other records listing Liofilchem 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: JWY)
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.