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FDA 510(k)

MTS Ciprofloxacin 0.002 - 32 µg/mL

K-Number: K183527 · 2019-03-19

Decision Date2019-03-19
Product CodeJWY
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

MTS Ciprofloxacin 0.002 - 32 µg/mL is a medical device manufactured by Liofilchem s.r.l.. It received FDA 510(k) clearance on 2019-03-19 under approval number K183527. 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 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. It is manufactured by Liofilchem s.r.l.. The 510(k) number is K183527.

When was MTS Ciprofloxacin 0.002 - 32 µg/mL approved by the FDA?

MTS Ciprofloxacin 0.002 - 32 µg/mL received FDA 510(k) clearance on 2019-03-19, under approval number K183527.

What company makes MTS Ciprofloxacin 0.002 - 32 µg/mL?

MTS Ciprofloxacin 0.002 - 32 µg/mL is manufactured by Liofilchem s.r.l..

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 Devices by Liofilchem s.r.l.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.