The following data is part of a premarket notification filed by Sensititre Ltd. with the FDA for Sensititre 18 Hour Susceptibility Plates.
| Device ID | K960220 |
| 510k Number | K960220 |
| Device Name: | SENSITITRE 18 HOUR SUSCEPTIBILITY PLATES |
| Classification | Manual Antimicrobial Susceptibility Test Systems |
| Applicant | SENSITITRE LTD. 29299 CLEMENTS RD. SUITE 1K Westlake, OH 44145 |
| Contact | Rebecca D Fields |
| Correspondent | Rebecca D Fields SENSITITRE LTD. 29299 CLEMENTS RD. SUITE 1K Westlake, OH 44145 |
| Product Code | JWY |
| CFR Regulation Number | 866.1640 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1996-01-16 |
| Decision Date | 1996-03-11 |