Arbor Technologies, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 10
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K960928 | SYRINGEFILTER | April 4, 1997 |
| K964283 | AUTOPRIME | January 22, 1997 |
| K922777 | PRESSURE TUBING AND ACCESSORIES | March 22, 1994 |
| K902666 | ANESTHESIA CONDUCTION FILTER | April 23, 1991 |
| K895859 | CONTAIN(TM) | February 7, 1991 |
| K902167 | CONTAIN(TM) LASER PLUME FILTER | January 4, 1991 |
| K890844 | MICROSEPT 60/20 | June 7, 1989 |
| K874505 | CONTAIN(TM) | May 20, 1988 |
| K864113 | CLYDE (TM) FILTRATION SYSTEM | February 4, 1987 |
| K863162 | VACU-GUARD | August 29, 1986 |