The following data is part of a premarket notification filed by Diamed Division Ill. Tool Works, Inc. with the FDA for Touchless Home-cath.
| Device ID | K812281 |
| 510k Number | K812281 |
| Device Name: | TOUCHLESS HOME-CATH |
| Classification | Catheter, Urological |
| Applicant | DIAMED DIVISION ILL. TOOL WORKS, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | KOD |
| CFR Regulation Number | 876.5130 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1981-08-13 |
| Decision Date | 1981-10-13 |