The following data is part of a premarket notification filed by American Omni Medical, Inc. with the FDA for Cardiotomy Reservoir Valve No. Crv-30 Or Pcrv-25.
Device ID | K884893 |
510k Number | K884893 |
Device Name: | CARDIOTOMY RESERVOIR VALVE NO. CRV-30 OR PCRV-25 |
Classification | Accessory Equipment, Cardiopulmonary Bypass |
Applicant | AMERICAN OMNI MEDICAL, INC. 2930-G GRACE LN. Costa Mesa, CA 92626 |
Contact | George G Siposs |
Correspondent | George G Siposs AMERICAN OMNI MEDICAL, INC. 2930-G GRACE LN. Costa Mesa, CA 92626 |
Product Code | KRI |
CFR Regulation Number | 870.4200 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1988-11-22 |
Decision Date | 1989-01-30 |