The following data is part of a premarket notification filed by Sherwood Medical Industries with the FDA for Catheter, Umbilical Artery.
| Device ID | K760966 |
| 510k Number | K760966 |
| Device Name: | CATHETER, UMBILICAL ARTERY |
| Classification | Catheter, Umbilical Artery |
| Applicant | SHERWOOD MEDICAL INDUSTRIES 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | FOS |
| CFR Regulation Number | 880.5200 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1976-11-04 |
| Decision Date | 1977-01-26 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 10884527020539 | K760966 | 000 |
| 10884527020522 | K760966 | 000 |
| 10884527005130 | K760966 | 000 |