# Arbor Technologies, Inc.

- Location (FDA's records): Ann Arbor, MI
- FDA decisions: 10 (1986–1997): 10 510(k) clearances
- Product codes: FPB (2), GCX (2), BSN (2), CAK (1), HIF (1), JDY (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K960928: Syringefilter (Apr 4, 1997)
- K964283: Autoprime (Jan 22, 1997)
- K922777: Pressure Tubing and Accessories (Mar 22, 1994)
- K902666: Anesthesia Conduction Filter (Apr 23, 1991)
- K895859: Contain (TM) (Feb 7, 1991)
- K902167: Contain (TM) Laser Plume Filter (Jan 4, 1991)
- K890844: Microsept 60/20 (Jun 7, 1989)
- K874505: Contain (TM) (May 20, 1988)

Source page: https://510kreport.com/company/arbor-technologies