The following data is part of a premarket notification filed by Medi-plast Intl., Inc. with the FDA for Operating Room Tray Set.
| Device ID | K840021 |
| 510k Number | K840021 |
| Device Name: | OPERATING ROOM TRAY SET |
| Classification | Tray, Surgical, Instrument |
| Applicant | MEDI-PLAST INTL., INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | FSM |
| CFR Regulation Number | 878.4800 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1984-01-05 |
| Decision Date | 1984-03-15 |