The following data is part of a premarket notification filed by California Medical Laboratories, Inc. with the FDA for Aortic Arch Cannulas.
Device ID | K943934 |
510k Number | K943934 |
Device Name: | AORTIC ARCH CANNULAS |
Classification | Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass |
Applicant | CALIFORNIA MEDICAL LABORATORIES, INC. P.O. BOX 18470 Irvine, CA 92713 |
Contact | Mehmet Bicakci |
Correspondent | Mehmet Bicakci CALIFORNIA MEDICAL LABORATORIES, INC. P.O. BOX 18470 Irvine, CA 92713 |
Product Code | DWF |
CFR Regulation Number | 870.4210 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1994-08-12 |
Decision Date | 1995-06-02 |