The following data is part of a premarket notification filed by Puritan Bennett Corp. with the FDA for Nellcor Puritan Bennett, 740 Ventilator System.
| Device ID | K964540 |
| 510k Number | K964540 |
| Device Name: | NELLCOR PURITAN BENNETT, 740 VENTILATOR SYSTEM |
| Classification | Ventilator, Continuous, Facility Use |
| Applicant | PURITAN BENNETT CORP. 2200 FARADAY AVE. Carlsbad, CA 92008 |
| Contact | Ann-marie Butler |
| Correspondent | Ann-marie Butler PURITAN BENNETT CORP. 2200 FARADAY AVE. Carlsbad, CA 92008 |
| Product Code | CBK |
| CFR Regulation Number | 868.5895 [🔎] |
| Decision | Se Subject To Tracking Reg (ST) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1996-11-12 |
| Decision Date | 1997-11-14 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 20884521113777 | K964540 | 000 |
| 10884521183155 | K964540 | 000 |