The following data is part of a premarket notification filed by 3m Medical Products Group with the FDA for 3m Laser Imager Model 969.
| Device ID | K923075 |
| 510k Number | K923075 |
| Device Name: | 3M LASER IMAGER MODEL 969 |
| Classification | Camera, Multi Format, Radiological |
| Applicant | 3M MEDICAL PRODUCTS GROUP 3M CENTER, BLDG. 275-3E-08 St. Paul, MN 55144 -1000 |
| Contact | John A Gravelle |
| Correspondent | John A Gravelle 3M MEDICAL PRODUCTS GROUP 3M CENTER, BLDG. 275-3E-08 St. Paul, MN 55144 -1000 |
| Product Code | LMC |
| CFR Regulation Number | 892.2040 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1992-06-25 |
| Decision Date | 1992-09-23 |