510(k) K191809

MTS Imipenem-relebactam 0.002/4-32/4 µg/mL by Liofilchem s.r.l. — Product Code JWY

K191809 is an FDA 510(k) premarket notification submitted by Liofilchem s.r.l. for the device "MTS Imipenem-relebactam 0.002/4-32/4 µg/mL". The FDA issued a decision of Substantially Equivalent on August 23, 2019. The device falls under product code JWY (Manual Antimicrobial Susceptibility Test Systems), a Class II device regulated under 21 CFR 866.1640. Liofilchem s.r.l. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 23, 2019
Date Received
July 5, 2019
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Manual Antimicrobial Susceptibility Test Systems
Device Class
Class II
Regulation Number
866.1640
Review Panel
MI
Submission Type