The following data is part of a premarket notification filed by Carwild Corp. with the FDA for Suture Removal Kits Sterile.
| Device ID | K833688 |
| 510k Number | K833688 |
| Device Name: | SUTURE REMOVAL KITS STERILE |
| Classification | Tape And Bandage, Adhesive |
| Applicant | CARWILD CORP. 4221 Richmond Rd., N.W. Walker, MI 49534 |
| Product Code | KGX |
| CFR Regulation Number | 880.5240 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1983-10-31 |
| Decision Date | 1984-05-31 |