QUATTRO AIR
Ventilator, Non-continuous (respirator)
RESMED LTD.
The following data is part of a premarket notification filed by Resmed Ltd. with the FDA for Quattro Air.
Pre-market Notification Details
| Device ID | K123979 |
| 510k Number | K123979 |
| Device Name: | QUATTRO AIR |
| Classification | Ventilator, Non-continuous (respirator) |
| Applicant | RESMED LTD. 9001 SPECTRUM CENTER BLVD. San Diego, CA 92123 |
| Contact | Jim Cassi |
| Correspondent | Jim Cassi RESMED LTD. 9001 SPECTRUM CENTER BLVD. San Diego, CA 92123 |
| Product Code | BZD |
| CFR Regulation Number | 868.5905 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2012-12-26 |
| Decision Date | 2013-02-27 |
| Summary: | summary |
Trademark Results [QUATTRO AIR]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 QUATTRO AIR 85816797 4530535 Live/Registered |
RESMED PTY LTD 2013-01-07 |
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