The following data is part of a premarket notification filed by Sherwood Medical Co. with the FDA for Argyle Polyurethane Umbilical Vessel Catheter.
| Device ID | K850884 |
| 510k Number | K850884 |
| Device Name: | ARGYLE POLYURETHANE UMBILICAL VESSEL CATHETER |
| Classification | Catheter, Umbilical Artery |
| Applicant | SHERWOOD MEDICAL CO. 1915 OLIVE ST. St. Louis, MO 63103 -1625 |
| Contact | Frank J Fucile |
| Correspondent | Frank J Fucile SHERWOOD MEDICAL CO. 1915 OLIVE ST. St. Louis, MO 63103 -1625 |
| Product Code | FOS |
| CFR Regulation Number | 880.5200 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1985-03-04 |
| Decision Date | 1985-10-17 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 20884527005168 | K850884 | 000 |
| 20884527005151 | K850884 | 000 |