The following data is part of a premarket notification filed by Snyder Laboratories, Inc. with the FDA for Tray, Urethral Catheterization.
| Device ID | K790272 |
| 510k Number | K790272 |
| Device Name: | TRAY, URETHRAL CATHETERIZATION |
| Classification | Tray, Catheterization, Sterile Urethral, With Or Without Catheter (kit) |
| Applicant | SNYDER LABORATORIES, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | FCM |
| CFR Regulation Number | 876.5130 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1979-01-13 |
| Decision Date | 1979-03-06 |