The following data is part of a premarket notification filed by Drager Medizintechnik Gmbh with the FDA for Ventview, Model 8414095.
Device ID | K012177 |
510k Number | K012177 |
Device Name: | VENTVIEW, MODEL 8414095 |
Classification | Ventilator, Continuous, Facility Use |
Applicant | DRAGER MEDIZINTECHNIK GMBH 3135 QUARRY RD. Telford, PA 18969 |
Contact | James J Brennan |
Correspondent | James J Brennan DRAGER MEDIZINTECHNIK GMBH 3135 QUARRY RD. Telford, PA 18969 |
Product Code | CBK |
CFR Regulation Number | 868.5895 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2001-07-12 |
Decision Date | 2001-09-04 |
Summary: | summary |