The following data is part of a premarket notification filed by Customed, Inc. with the FDA for Sterile Suture Removal Kit.
| Device ID | K925015 |
| 510k Number | K925015 |
| Device Name: | STERILE SUTURE REMOVAL KIT |
| Classification | Suture Removal Kit |
| 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 | MCZ |
| CFR Regulation Number | 878.4800 [🔎] |
| Decision | Substantially Equivalent - Kit (SESK) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1992-09-24 |
| Decision Date | 1993-06-07 |