The following data is part of a premarket notification filed by Sensititre Alamar with the FDA for Sensititre 18 Hour Susceptibility Plates.
Device ID | K962867 |
510k Number | K962867 |
Device Name: | SENSITITRE 18 HOUR SUSCEPTIBILITY PLATES |
Classification | Manual Antimicrobial Susceptibility Test Systems |
Applicant | SENSITITRE ALAMAR 29299 CLEMENS RD. SUITE 1K Westlake, OH 44145 |
Contact | Rebecca D Fields |
Correspondent | Rebecca D Fields SENSITITRE ALAMAR 29299 CLEMENS 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 | 1996-07-23 |
Decision Date | 1996-09-30 |