# Resmed Pty Ltd (Registration Number: 3004604967)

- Location (FDA's records): Bella Vista, AU
- FDA decisions: 3 (2023–2024): 3 510(k) clearances
- Product codes: BZD (3)
- 510(k) review time since 2016: median 239 days, against 204 for FDA's reviews in the same codes and years (0 of 3 faster)
- Predicates its devices cite: 3 (0 its own); citations of its devices by later devices: 1 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Resmed, Ltd.: 3 (https://510kreport.com/company/resmed)

## Firms that cite its devices most
- BMC Medical Co., Ltd.: 1 (https://510kreport.com/company/bmc-medical)

## Its most-cited devices
- K234134: AirFit F30i Mask System; AirFit F30i NM Mask System; Arcadia Mask System (2024), cited by 1

## Recent decisions
- K234134: AirFit F30i Mask System; AirFit F30i NM Mask System; Arcadia Mask System (Sep 24, 2024)
- K230476: Oran Park Mask (Oct 19, 2023)
- K223747: Whitsundays Mask System (Jul 6, 2023)

Source page: https://510kreport.com/company/resmed-registration-number-3004604967