The following data is part of a premarket notification filed by Radionics, Inc. with the FDA for Wireless Standard Probe, Dynamic Reference Frame (drf).
| Device ID | K982364 |
| 510k Number | K982364 |
| Device Name: | WIRELESS STANDARD PROBE, DYNAMIC REFERENCE FRAME (DRF) |
| Classification | Neurological Stereotaxic Instrument |
| Applicant | RADIONICS, INC. 22 TERRY AVE. Burlington, MA 01803 -2516 |
| Contact | Lisa Misterka Benati |
| Correspondent | Lisa Misterka Benati RADIONICS, INC. 22 TERRY AVE. Burlington, MA 01803 -2516 |
| Product Code | HAW |
| CFR Regulation Number | 882.4560 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1998-07-06 |
| Decision Date | 1998-08-05 |
| Summary: | summary |