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 |