# Optovent AB

- Location (FDA's records): Fort Lee, NJ
- FDA decisions: 2 (1999–2001): 2 510(k) clearances
- Names in FDA's records: Optovent AB (1); Optovent, Inc. (1)
- Product codes: BZQ (2)
- 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
- K003704: Optovent Respons, Optovent Renee (Optovent Respons Without Pulse Oximetry Module) (Feb 5, 2001)
- K981725: Optovent Respiratory Monitor Model Number RR 9700 (Feb 2, 1999)

Source page: https://510kreport.com/company/optovent