The following data is part of a premarket notification filed by Northgate Research, Inc. with the FDA for 5f Electrode(lithotriptor).
| Device ID | K852874 |
| 510k Number | K852874 |
| Device Name: | 5F ELECTRODE(LITHOTRIPTOR) |
| Classification | Lithotriptor, Electro-hydraulic |
| Applicant | NORTHGATE RESEARCH, INC. P.O. BOX 978 Plattsburgh, NJ 12901 |
| Contact | James A Cochie |
| Correspondent | James A Cochie NORTHGATE RESEARCH, INC. P.O. BOX 978 Plattsburgh, NJ 12901 |
| Product Code | FFK |
| CFR Regulation Number | 876.4480 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1985-07-08 |
| Decision Date | 1985-08-21 |