The following data is part of a premarket notification filed by Life Corp. with the FDA for Life O2.
| Device ID | K910201 | 
| 510k Number | K910201 | 
| Device Name: | LIFE O2 | 
| Classification | Ventilator, Emergency, Powered (resuscitator) | 
| Applicant | LIFE CORP. P.O. BOX 300 W140 N5566 LILLY ROAD Menomonee Falls, WI 53051 | 
| Contact | John Kirchgeorg | 
| Correspondent | John Kirchgeorg LIFE CORP. P.O. BOX 300 W140 N5566 LILLY ROAD Menomonee Falls, WI 53051 | 
| Product Code | BTL | 
| CFR Regulation Number | 868.5925 [🔎] | 
| Decision | Substantially Equivalent (SESE) | 
| Type | Traditional | 
| 3rd Party Reviewed | No | 
| Combination Product | No | 
| Date Received | 1991-01-18 | 
| Decision Date | 1991-02-01 | 
| Mark Image Registration | Serial | Company Trademark Application Date | 
|---|---|
|  LIFE O2  74710285  2369634 Dead/Cancelled | LIFE INTERNATIONAL PRODUCTS, INC. 1995-08-02 |