The following data is part of a premarket notification filed by 3m Health Care, Sarns with the FDA for Sarns Retrograde Cannula.
Device ID | K925442 |
510k Number | K925442 |
Device Name: | SARNS RETROGRADE CANNULA |
Classification | Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass |
Applicant | 3M HEALTH CARE, SARNS 6200 JACKSON RD. PO BOX 1247 Ann Arbor, MI 48106 |
Contact | Nelson L Huldin |
Correspondent | Nelson L Huldin 3M HEALTH CARE, SARNS 6200 JACKSON RD. PO BOX 1247 Ann Arbor, MI 48106 |
Product Code | DWF |
CFR Regulation Number | 870.4210 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1992-10-28 |
Decision Date | 1993-05-21 |