Anatech, Ltd.
Anatech, Ltd. appears in FDA public data with 0 recalls, 14 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on July 28, 1988.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 14
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K882874 | ZINC FORMALIN | July 28, 1988 |
| K882873 | FIELDTEX HEMATOXYLIN | July 28, 1988 |
| K882268 | ZINC FORMALIN CONCENTRATE | June 15, 1988 |
| K881282 | XYLENE | April 5, 1988 |
| K872663 | DRY-FORM | August 6, 1987 |
| K872500 | ANATECH HEMATOXYLIN-EXTRA STRENGTH | July 9, 1987 |
| K872498 | HARRIS HEMATOXYLIN | July 9, 1987 |
| K872499 | ANATECH HEMATOXYLIN-NORMAL STRENGTH | July 9, 1987 |
| K870852 | NBF 10% NEUTRAL BUFFERED FORMALIN | March 31, 1987 |
| K842862 | CB FORMALIN | August 28, 1984 |
| K842940 | CBA FORMALIN | August 28, 1984 |
| K842863 | PRO-SOFT DEHYDRANT | August 21, 1984 |
| K842861 | PRO-PAR CLEARANT | August 21, 1984 |
| K842986 | REFRAX MOUNTING MEDIUM | August 21, 1984 |