The following data is part of a premarket notification filed by Oxoid U.s.a., Inc. with the FDA for Campylobacter Blood-free Selective Agar Base.
Device ID | K850658 |
510k Number | K850658 |
Device Name: | CAMPYLOBACTER BLOOD-FREE SELECTIVE AGAR BASE |
Classification | Culture Media, Non-selective And Non-differential |
Applicant | OXOID U.S.A., INC. 9017 RED BRANCH RD. Columbia, MD 21045 |
Contact | Ruth Kemp |
Correspondent | Ruth Kemp OXOID U.S.A., INC. 9017 RED BRANCH RD. Columbia, MD 21045 |
Product Code | JSG |
CFR Regulation Number | 866.2300 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1985-02-15 |
Decision Date | 1985-03-20 |
Device Identifier | submissionNumber | Supplement |
---|---|---|
05032384003990 | K850658 | 000 |