The following data is part of a premarket notification filed by Joe W. Utt with the FDA for Valve, Anti-syphon Model Pudenze Flush..
| Device ID | K760502 |
| 510k Number | K760502 |
| Device Name: | VALVE, ANTI-SYPHON MODEL PUDENZE FLUSH. |
| Classification | Shunt, Central Nervous System And Components |
| Applicant | JOE W. UTT 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | JXG |
| CFR Regulation Number | 882.5550 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1976-08-23 |
| Decision Date | 1976-08-30 |