The following data is part of a premarket notification filed by Sherwood Medical Co. with the FDA for Argyle Pvc Feeding Tube.
| Device ID | K820441 |
| 510k Number | K820441 |
| Device Name: | ARGYLE PVC FEEDING TUBE |
| Classification | Tubes, Gastrointestinal (and Accessories) |
| Applicant | SHERWOOD MEDICAL CO. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | KNT |
| CFR Regulation Number | 876.5980 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1982-02-18 |
| Decision Date | 1982-03-10 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 40884521003768 | K820441 | 000 |
| 40884521003614 | K820441 | 000 |
| 40884521003232 | K820441 | 000 |
| 40884521003218 | K820441 | 000 |
| 10884521067363 | K820441 | 000 |