The following data is part of a premarket notification filed by Respironics California, Inc. with the FDA for V200 Ventilator With Aprv Mode, Esprit Ventilator With Aprv Mode.
Device ID | K110083 |
510k Number | K110083 |
Device Name: | V200 VENTILATOR WITH APRV MODE, ESPRIT VENTILATOR WITH APRV MODE |
Classification | Ventilator, Continuous, Facility Use |
Applicant | RESPIRONICS CALIFORNIA, INC. 2271 COSMOS CT. Carlsbad, CA 92130 |
Contact | Mary Funk |
Correspondent | Mary Funk RESPIRONICS CALIFORNIA, INC. 2271 COSMOS CT. Carlsbad, CA 92130 |
Product Code | CBK |
CFR Regulation Number | 868.5895 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2011-01-11 |
Decision Date | 2012-01-13 |
Summary: | summary |