The following data is part of a premarket notification filed by 3m Company with the FDA for Avi Model 2012, 1.2 Micron Filter Iv Administra..
| Device ID | K896161 |
| 510k Number | K896161 |
| Device Name: | AVI MODEL 2012, 1.2 MICRON FILTER IV ADMINISTRA. |
| Classification | Set, Administration, Intravascular |
| Applicant | 3M COMPANY 1120 RED FOX RD. St. Paul, MN 55112 |
| Contact | Von Busch |
| Correspondent | Von Busch 3M COMPANY 1120 RED FOX RD. St. Paul, MN 55112 |
| Product Code | FPA |
| CFR Regulation Number | 880.5440 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1989-10-24 |
| Decision Date | 1990-01-11 |