The following data is part of a premarket notification filed by Hardy Diagnostics with the FDA for M. Cat Butyrate Disk.
Device ID | K960996 |
510k Number | K960996 |
Device Name: | M. CAT BUTYRATE DISK |
Classification | Discs, Strips And Reagents, Microorganism Differentiation |
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 | JTO |
CFR Regulation Number | 866.2660 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1996-03-12 |
Decision Date | 1996-04-18 |
Device Identifier | submissionNumber | Supplement |
---|---|---|
00819398027267 | K960996 | 000 |