The following data is part of a premarket notification filed by Resmed Corp with the FDA for Vpap Adapt.
| Device ID | K113801 |
| 510k Number | K113801 |
| Device Name: | VPAP ADAPT |
| Classification | Ventilator, Non-continuous (respirator) |
| Applicant | RESMED CORP 9001 SPECTRUM CENTER BOULEVARD Kearny Mesa, CA 92123 |
| Contact | David D D'cruz |
| Correspondent | David D D'cruz RESMED CORP 9001 SPECTRUM CENTER BOULEVARD Kearny Mesa, 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 | 2011-12-22 |
| Decision Date | 2012-05-25 |
| Summary: | summary |