The following data is part of a premarket notification filed by Resmed Ltd. with the FDA for Vpap Iii St-a/kidsta Mask System.
| Device ID | K060105 |
| 510k Number | K060105 |
| Device Name: | VPAP III ST-A/KIDSTA MASK SYSTEM |
| Classification | Ventilator, Continuous, Non-life-supporting |
| Applicant | RESMED LTD. 14040 DANIELSON ST. Poway, CA 92064 -6857 |
| Contact | David D'cruz |
| Correspondent | David D'cruz RESMED LTD. 14040 DANIELSON ST. Poway, CA 92064 -6857 |
| Product Code | MNS |
| CFR Regulation Number | 868.5895 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2006-01-13 |
| Decision Date | 2006-04-07 |
| Summary: | summary |