Arbor Technologies, Inc.
Ann Arbor, MI, US
Arbor Technologies, Inc. appears in FDA device records in Ann Arbor, MI. FDA records list 10 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.
FDA records held for this company
- 510(k) clearances
- 10
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 10 510(k) clearances for Arbor Technologies, Inc. between 1986 and 1997. The busiest year on record is 1991, with 3. The most recent is 1997, with 2.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1986 | 1 |
| 1987 | 1 |
| 1988 | 1 |
| 1989 | 1 |
| 1991 | 3 |
| 1994 | 1 |
| 1997 | 2 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K960928 | SYRINGEFILTER | BSN | Substantially Equivalent | |
| K964283 | AUTOPRIME | FPB | Substantially Equivalent | |
| K922777 | PRESSURE TUBING AND ACCESSORIES | HIF | Substantially Equivalent | |
| K902666 | ANESTHESIA CONDUCTION FILTER | BSN | Substantially Equivalent | |
| K895859 | CONTAIN(TM) | GCX | Substantially Equivalent | |
| K902167 | CONTAIN(TM) LASER PLUME FILTER | JDY | Substantially Equivalent | |
| K890844 | MICROSEPT 60/20 | CAK | Substantially Equivalent | |
| K874505 | CONTAIN(TM) | GCX | Substantially Equivalent | |
| K864113 | CLYDE (TM) FILTRATION SYSTEM | FPB | Substantially Equivalent | |
| K863162 | VACU-GUARD | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
Recall records
No recall records for this company in the ingested FDA data.
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain