The following data is part of a premarket notification filed by American V. Mueller with the FDA for Effron Parotid Retractor.
| Device ID | K801759 |
| 510k Number | K801759 |
| Device Name: | EFFRON PAROTID RETRACTOR |
| Classification | Retractor |
| Applicant | AMERICAN V. MUELLER 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | GAD |
| CFR Regulation Number | 878.4800 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1980-07-28 |
| Decision Date | 1980-08-20 |