The following data is part of a premarket notification filed by Progress Mankind Technology with the FDA for Vaxiom Family Of Rf Lesion Probes & Elec.
| Device ID | K802243 |
| 510k Number | K802243 |
| Device Name: | VAXIOM FAMILY OF RF LESION PROBES & ELEC |
| Classification | Probe, Radiofrequency Lesion |
| Applicant | PROGRESS MANKIND TECHNOLOGY BOX 464 Hopkins, MN 55343 |
| Contact | Alfred A Iversen |
| Correspondent | Alfred A Iversen PROGRESS MANKIND TECHNOLOGY BOX 464 Hopkins, MN 55343 |
| Product Code | GXI |
| CFR Regulation Number | 882.4725 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1980-09-16 |
| Decision Date | 1980-11-12 |