The following data is part of a premarket notification filed by Trek Diagnostic Systems, Inc. with the FDA for Sensitire Susceptibility Plates- Additional Antimicrobics.
Device ID | K052091 |
510k Number | K052091 |
Device Name: | SENSITIRE SUSCEPTIBILITY PLATES- ADDITIONAL ANTIMICROBICS |
Classification | Manual Antimicrobial Susceptibility Test Systems |
Applicant | TREK DIAGNOSTIC SYSTEMS, INC. 982 KEYNOTE CIRCLE SUITE 6 Cleveland, OH 44131 |
Contact | Cynthia C Knapp |
Correspondent | Cynthia C Knapp TREK DIAGNOSTIC SYSTEMS, INC. 982 KEYNOTE CIRCLE SUITE 6 Cleveland, OH 44131 |
Product Code | JWY |
Subsequent Product Code | LRG |
Subsequent Product Code | LTT |
CFR Regulation Number | 866.1640 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2005-08-02 |
Decision Date | 2005-09-21 |