The following data is part of a premarket notification filed by Hardy Diagnostics with the FDA for Hardydisk Cefotetan, 30mcg.
Device ID | K002661 |
510k Number | K002661 |
Device Name: | HARDYDISK CEFOTETAN, 30MCG |
Classification | Susceptibility Test Discs, Antimicrobial |
Applicant | HARDY DIAGNOSTICS 1430 WEST MCCOY LN. Santa Maria, CA 93455 |
Contact | Melissa M Traylor |
Correspondent | Melissa M Traylor 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 | 2000-08-25 |
Decision Date | 2000-10-26 |
Device Identifier | submissionNumber | Supplement |
---|---|---|
00816576020454 | K002661 | 000 |