The following data is part of a premarket notification filed by Customed, Inc. with the FDA for Surgical Tray (sterile).
| Device ID | K925022 |
| 510k Number | K925022 |
| Device Name: | SURGICAL TRAY (STERILE) |
| Classification | Applicator, Ent Drug |
| Applicant | CUSTOMED, INC. CALLE IGUALDAD #7 Fajardo, PR 00738 |
| Contact | Felix B Santos |
| Correspondent | Felix B Santos CUSTOMED, INC. CALLE IGUALDAD #7 Fajardo, PR 00738 |
| Product Code | LRD |
| CFR Regulation Number | 874.5220 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1992-09-24 |
| Decision Date | 1993-04-26 |