The following data is part of a premarket notification filed by Vital Signs, Inc. with the FDA for Breas Pv 10i Cpap System, Model Pv 10i.
| Device ID | K030985 |
| 510k Number | K030985 |
| Device Name: | BREAS PV 10I CPAP SYSTEM, MODEL PV 10I |
| Classification | Ventilator, Non-continuous (respirator) |
| Applicant | VITAL SIGNS, INC. 20 CAMPUS RD. Totowa, NJ 07512 |
| Contact | Anthony P Martino |
| Correspondent | Anthony P Martino VITAL SIGNS, INC. 20 CAMPUS RD. Totowa, NJ 07512 |
| Product Code | BZD |
| CFR Regulation Number | 868.5905 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2003-03-28 |
| Decision Date | 2003-10-15 |
| Summary: | summary |