K251879

Sulopenem SPM 2 µg

510(k) number
K251879
Device name
Sulopenem SPM 2 µg
Applicant
Liofilchem MA · US
Product code
JTN — Susceptibility Test Discs, Antimicrobial
Decision date
2025-08-12
Date received
2025-06-18
Decision
Substantially Equivalent
Clearance type
Traditional
Advisory committee
Microbiology
This submission filed a 510(k) Statement rather than a Summary; no public summary is available from FDA.
Official FDA record: K251879
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.