LIQUID OXYGEN SYSTEM
Unit, Liquid-oxygen, Portable
PURITAN BENNETT CORP.
The following data is part of a premarket notification filed by Puritan Bennett Corp. with the FDA for Liquid Oxygen System.
Pre-market Notification Details
| Device ID | K830498 |
| 510k Number | K830498 |
| Device Name: | LIQUID OXYGEN SYSTEM |
| Classification | Unit, Liquid-oxygen, Portable |
| Applicant | PURITAN BENNETT CORP. 4221 Richmond Rd., N.W. Walker, MI 49534 |
| Product Code | BYJ |
| CFR Regulation Number | 868.5655 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1983-02-16 |
| Decision Date | 1983-03-10 |
NIH GUDID Devices
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