MTS Ciprofloxacin 0.002 - 32 µg/mL
K-Number: K183527 · 2019-03-19
Device Summary
Frequently Asked Questions
What is the MTS Ciprofloxacin 0.002 - 32 µg/mL?
MTS Ciprofloxacin 0.002 - 32 µg/mL is a medical device that received FDA 510(k) clearance on 2019-03-19. The listed applicant is Liofilchem s.r.l.. The 510(k) number is K183527.
When did MTS Ciprofloxacin 0.002 - 32 µg/mL receive FDA 510(k) clearance?
MTS Ciprofloxacin 0.002 - 32 µg/mL received FDA 510(k) clearance on 2019-03-19, under 510(k) number K183527.
Who is the listed applicant for MTS Ciprofloxacin 0.002 - 32 µg/mL?
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 MTS Ciprofloxacin 0.002 - 32 µg/mL?
The FDA product code for MTS Ciprofloxacin 0.002 - 32 µg/mL 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.