The following data is part of a premarket notification filed by Central Media with the FDA for General Purpose Media W/select. & Diff. Modifica..
Device ID | K873257 |
510k Number | K873257 |
Device Name: | GENERAL PURPOSE MEDIA W/SELECT. & DIFF. MODIFICA. |
Classification | Culture Media, Non-selective And Non-differential |
Applicant | CENTRAL MEDIA 10386 ROCKINGHAM DR. Sacramento, CA 95827 |
Contact | Rebecca Clark |
Correspondent | Rebecca Clark CENTRAL MEDIA 10386 ROCKINGHAM DR. Sacramento, CA 95827 |
Product Code | JSG |
CFR Regulation Number | 866.2300 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1987-08-11 |
Decision Date | 1987-11-06 |