The following data is part of a premarket notification filed by Hogan & Hartson with the FDA for I.m Probes.
| Device ID | K802951 |
| 510k Number | K802951 |
| Device Name: | I.M PROBES |
| Classification | Probe |
| Applicant | HOGAN & HARTSON 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | HXB |
| CFR Regulation Number | 888.4540 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1980-11-20 |
| Decision Date | 1980-12-17 |