The following data is part of a premarket notification filed by Respironics California, Inc. with the FDA for V200 Ventilator.
| Device ID | K102054 |
| 510k Number | K102054 |
| Device Name: | V200 VENTILATOR |
| Classification | Ventilator, Continuous, Facility Use |
| Applicant | RESPIRONICS CALIFORNIA, INC. 2271 COSMOS CT. Carlsbad, CA 92011 |
| Contact | Tamatha Ley |
| Correspondent | Tamatha Ley RESPIRONICS CALIFORNIA, INC. 2271 COSMOS CT. Carlsbad, CA 92011 |
| Product Code | CBK |
| CFR Regulation Number | 868.5895 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2010-07-22 |
| Decision Date | 2010-12-22 |
| Summary: | summary |