Company ยท US
Culture Kits, Inc.
FDA 510(k) clearances and medical device recalls filed under this name, 1985 to 1991. Name variants (Inc, Corp, punctuation) are merged.
9510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
| Code | Device | Records |
|---|---|---|
| JSI | Culture Media, Selective And Differential | 3 |
| JTZ | Culture Media, Antimicrobial Susceptibility Test, Mueller Hinton Agar/Broth | 2 |
| JSG | Culture Media, Non-Selective And Non-Differential | 1 |
| JSJ | Culture Media, Selective And Non-Differential | 1 |
| JSX | Kit, Identification, Neisseria Gonorrhoeae | 1 |
| JXA | Kit, Screening, Urine | 1 |
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Oct 4, 1991 | K911846 | URI-THREE(TM), MODIFICATION Culture Kits, Inc. | JXA |
| Jul 11, 1986 | K854672 | CANDI-KIT TM Culture Kits, Inc. | JSI |
| Aug 28, 1985 | K853488 | STAPH KIT Culture Kits, Inc. | JSI |
| Aug 13, 1985 | K851225 | URINE DUO Culture Kits, Inc. | JTZ |
| Jul 12, 1985 | K852582 | GONI-KIT Culture Kits, Inc. | JSX |
| Jul 9, 1985 | K852480 | DERM-KIT Culture Kits, Inc. | JSI |
| Apr 29, 1985 | K851518 | MUELLER HINTON SENSITIVITY PLATE Culture Kits, Inc. | JTZ |
| Apr 24, 1985 | K850765 | STREP-KIT Culture Kits, Inc. | JSJ |
| Apr 1, 1985 | K850998 | URI-KIT Culture Kits, Inc. | JSG |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||