The following data is part of a premarket notification filed by Flow Laboratories, Inc. with the FDA for Accessory Media For Flow Titertek Mic.
Device ID | K822119 |
510k Number | K822119 |
Device Name: | ACCESSORY MEDIA FOR FLOW TITERTEK MIC |
Classification | Culture Media, Antimicrobial Susceptibility Test, Mueller Hinton Agar/broth |
Applicant | FLOW LABORATORIES, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
Product Code | JTZ |
CFR Regulation Number | 866.1700 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1982-07-19 |
Decision Date | 1982-08-03 |