Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

ComASP Cefiderocol 0.008-128

K-Number: K230479 · 2023-05-18

Decision Date2023-05-18
Product CodeJWY
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

ComASP Cefiderocol 0.008-128 is the device name listed in this FDA 510(k) record. The listed applicant is Liofilchem s.r.l.. It received FDA 510(k) clearance on 2023-05-18 under 510(k) number K230479. The device is classified under product code JWY. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 35 devices →

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.