The following data is part of a premarket notification filed by Medical Plastics, Inc. with the FDA for Mpi Mon-it Ii, Smart Safety System.
| Device ID | K821169 |
| 510k Number | K821169 |
| Device Name: | MPI MON-IT II, SMART SAFETY SYSTEM |
| Classification | Electrosurgical, Cutting & Coagulation & Accessories |
| Applicant | MEDICAL PLASTICS, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | GEI |
| CFR Regulation Number | 878.4400 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1982-04-26 |
| Decision Date | 1982-08-06 |