The following data is part of a premarket notification filed by Diemolding Corp. with the FDA for Filter, Vacuum Line Lineguard.
| Device ID | K760420 |
| 510k Number | K760420 |
| Device Name: | FILTER, VACUUM LINE LINEGUARD |
| Classification | System, Simulation, Radiation Therapy |
| Applicant | DIEMOLDING CORP. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | KPQ |
| CFR Regulation Number | 892.5840 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1976-08-06 |
| Decision Date | 1976-08-23 |