The following data is part of a premarket notification filed by American V. Mueller with the FDA for V. Mueller Vital Clip-hemostatic Clip.
Device ID | K861471 |
510k Number | K861471 |
Device Name: | V. MUELLER VITAL CLIP-HEMOSTATIC CLIP |
Classification | Clip, Implantable |
Applicant | AMERICAN V. MUELLER 6600 W. TOUHY Chicago, IL 60648 |
Contact | Matthew Nowland |
Correspondent | Matthew Nowland AMERICAN V. MUELLER 6600 W. TOUHY Chicago, IL 60648 |
Product Code | FZP |
CFR Regulation Number | 878.4300 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1986-04-22 |
Decision Date | 1986-06-06 |