KOX — Solvent, Adhesive Tape Class I
FDA Device Classification
Classification Details
- Product Code
- KOX
- Device Class
- Class I
- Regulation Number
- 878.4730
- Submission Type
- Review Panel
- SU
- Medical Specialty
- General, Plastic Surgery
- Implant
- No
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
| K934790 | medi-flex hospital products | SEPP ADHESIVE REMOVER | March 11, 1994 |
| K931933 | chad labs | CHAD LABS ADHESIVE BANDAGE REMOVER | July 8, 1993 |
| K924976 | convatec, a division of e.r. squibb and sons | ALLKARE(TM) ADHESIVE REMOVER WIPE | April 20, 1993 |
| K924571 | orange-sol | MEDI-SOL | April 6, 1993 |
| K925618 | 3m health care | 3M REMOVER LOTION PRODUCT NUMBER 86XX | March 31, 1993 |
| K923351 | coloplast | SKIN SUPPORT PREP PAD | September 14, 1992 |
| K915150 | smith and nephew united | REMOVE ADHESIVE REMOVER | January 9, 1992 |
| K902009 | elantec | ELANTEC'S SURGICAL TAPE REMOVER | August 29, 1990 |
| K895293 | kemi labs | KEMI LABS - ADHESIVE BANDAGE REMOVER | February 9, 1990 |
| K893603 | smith and nephew united | REMOVE ADHESIVE REMOVER | July 14, 1989 |
| K881359 | stephens scientific | DECALCIFYING SOLUTION II | April 19, 1988 |
| K821162 | healthcare group laboratories | ADHESIVE REMOVER | May 14, 1982 |