The following data is part of a premarket notification filed by Respironics, Inc. with the FDA for Bipap Synchrony.
Device ID | K063533 |
510k Number | K063533 |
Device Name: | BIPAP SYNCHRONY |
Classification | Ventilator, Continuous, Non-life-supporting |
Applicant | RESPIRONICS, INC. 1001 MURRY RIDGE LN. Murrysville, PA 15668 |
Contact | Zita A Yurko |
Correspondent | Zita A Yurko RESPIRONICS, INC. 1001 MURRY RIDGE LN. Murrysville, PA 15668 |
Product Code | MNS |
CFR Regulation Number | 868.5895 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Abbreviated |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2006-11-22 |
Decision Date | 2007-02-20 |
Summary: | summary |