The following data is part of a premarket notification filed by Remel Co. with the FDA for Haemophilus I.d. Ii Triplate.
| Device ID | K840338 |
| 510k Number | K840338 |
| Device Name: | HAEMOPHILUS I.D. II TRIPLATE |
| Classification | Culture Media, Selective And Differential |
| Applicant | REMEL CO. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | JSI |
| CFR Regulation Number | 866.2360 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1984-01-25 |
| Decision Date | 1984-04-17 |