The following data is part of a premarket notification filed by Hardy Diagnostics with the FDA for Hardkydisk Neomycin, 30 Mcg.
Device ID | K011385 |
510k Number | K011385 |
Device Name: | HARDKYDISK NEOMYCIN, 30 MCG |
Classification | Susceptibility Test Discs, Antimicrobial |
Applicant | HARDY DIAGNOSTICS 1430 WEST MCCOY LN. Santa Maria, CA 93455 |
Contact | Melissa M Traylor, Rac |
Correspondent | Melissa M Traylor, Rac HARDY DIAGNOSTICS 1430 WEST MCCOY LN. Santa Maria, CA 93455 |
Product Code | JTN |
CFR Regulation Number | 866.1620 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2001-05-07 |
Decision Date | 2001-05-18 |