The following data is part of a premarket notification filed by Sherwood Medical Industries with the FDA for Catheter, Intravascular (medicut T).
| Device ID | K760163 |
| 510k Number | K760163 |
| Device Name: | CATHETER, INTRAVASCULAR (MEDICUT T) |
| Classification | Catheter, Intravascular, Therapeutic, Short-term Less Than 30 Days |
| Applicant | SHERWOOD MEDICAL INDUSTRIES 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | FOZ |
| CFR Regulation Number | 880.5200 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1976-06-30 |
| Decision Date | 1976-07-20 |