The following data is part of a premarket notification filed by Hardy Media with the FDA for Motility Test Medium.
Device ID | K821595 |
510k Number | K821595 |
Device Name: | MOTILITY TEST MEDIUM |
Classification | Culture Media, Non-selective And Differential |
Applicant | HARDY MEDIA 803 N. Front St. Suite 3 Mchenry, IL 60050 |
Product Code | JSH |
CFR Regulation Number | 866.2320 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1982-05-20 |
Decision Date | 1982-07-08 |