The following data is part of a premarket notification filed by Accumed Intl., Inc. with the FDA for Sensititre Haemophilus/streptococcus Pneumoniae Mic Plate.
Device ID | K965190 |
510k Number | K965190 |
Device Name: | SENSITITRE HAEMOPHILUS/STREPTOCOCCUS PNEUMONIAE MIC PLATE |
Classification | Manual Antimicrobial Susceptibility Test Systems |
Applicant | ACCUMED INTL., INC. 29299 CLEMENS RD. SUITE 1K Westlake, OH 44145 |
Contact | Cynthia C Knapp |
Correspondent | Cynthia C Knapp ACCUMED INTL., INC. 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 | 1996-12-24 |
Decision Date | 1997-03-19 |