The following data is part of a premarket notification filed by Remel Co. with the FDA for Ef Synergy Quad.
| Device ID | K903589 |
| 510k Number | K903589 |
| Device Name: | EF SYNERGY QUAD |
| Classification | Manual Antimicrobial Susceptibility Test Systems |
| Applicant | REMEL CO. 12076 SANTA FE DR. Lenexa, KS 66215 |
| Contact | Ann Silvius |
| Correspondent | Ann Silvius REMEL CO. 12076 SANTA FE DR. Lenexa, KS 66215 |
| Product Code | JWY |
| CFR Regulation Number | 866.1640 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1990-08-08 |
| Decision Date | 1990-11-13 |