The following data is part of a premarket notification filed by Life Corp. with the FDA for Life Oxygenpac For Trained Medical Personnel.
Device ID | K910434 |
510k Number | K910434 |
Device Name: | LIFE OXYGENPAC FOR TRAINED MEDICAL PERSONNEL |
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 | 1991-01-31 |
Decision Date | 1991-06-17 |