The following data is part of a premarket notification filed by Liofilchem S. R. L. with the FDA for Mts Penicillin 0.002- 32 µg/ml.
Device ID | K181889 |
510k Number | K181889 |
Device Name: | MTS Penicillin 0.002- 32 µg/mL |
Classification | Manual Antimicrobial Susceptibility Test Systems |
Applicant | Liofilchem S. R. L. Via Scozia Zona Ind.le Roseto Degli Abruzzi, IT 64026 |
Contact | Fabio Brocco |
Correspondent | Laura M. Koeth Laboratory Specialists, Inc 26214 Center Ridge Road Westlake, OH 44145 |
Product Code | JWY |
CFR Regulation Number | 866.1640 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2018-07-13 |
Decision Date | 2018-09-13 |
Device Identifier | submissionNumber | Supplement |
---|---|---|
08055182872855 | K181889 | 000 |