The following data is part of a premarket notification filed by Viasys Respiratory Care Inc with the FDA for Modification To Avea Ventilator.
Device ID | K073069 |
510k Number | K073069 |
Device Name: | MODIFICATION TO AVEA VENTILATOR |
Classification | Ventilator, Continuous, Facility Use |
Applicant | VIASYS RESPIRATORY CARE INC 1100 BIRD CENTER DR. Palm Springs, CA 92262 |
Contact | Tom Gutierrez |
Correspondent | Tom Gutierrez VIASYS RESPIRATORY CARE INC 1100 BIRD CENTER DR. Palm Springs, CA 92262 |
Product Code | CBK |
CFR Regulation Number | 868.5895 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2007-10-30 |
Decision Date | 2008-01-25 |
Summary: | summary |