The following data is part of a premarket notification filed by Sherwood Medical Co. with the FDA for Argyle Yankaver Suction Tube W/control.
| Device ID | K832027 |
| 510k Number | K832027 |
| Device Name: | ARGYLE YANKAVER SUCTION TUBE W/CONTROL |
| Classification | Catheter And Tip, Suction |
| Applicant | SHERWOOD MEDICAL CO. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | JOL |
| CFR Regulation Number | 880.6740 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1983-06-23 |
| Decision Date | 1983-08-08 |