Culture Kits, Inc.
Culture Kits, Inc. appears in FDA public data with 0 recalls, 9 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on October 4, 1991.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 9
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K911846 | URI-THREE(TM), MODIFICATION | October 4, 1991 |
| K854672 | CANDI-KIT TM | July 11, 1986 |
| K853488 | STAPH KIT | August 28, 1985 |
| K851225 | URINE DUO | August 13, 1985 |
| K852582 | GONI-KIT | July 12, 1985 |
| K852480 | DERM-KIT | July 9, 1985 |
| K851518 | MUELLER HINTON SENSITIVITY PLATE | April 29, 1985 |
| K850765 | STREP-KIT | April 24, 1985 |
| K850998 | URI-KIT | April 1, 1985 |