The following data is part of a premarket notification filed by Northgate Technologies, Inc. with the FDA for 1.9 French Lithotripter Electrode, Modification.
| Device ID | K914514 |
| 510k Number | K914514 |
| Device Name: | 1.9 FRENCH LITHOTRIPTER ELECTRODE, MODIFICATION |
| Classification | Lithotriptor, Electro-hydraulic |
| Applicant | NORTHGATE TECHNOLOGIES, INC. 3930 VENTURA DR. Arlington Heights, IL 60004 |
| Contact | Scott K Gilchrist |
| Correspondent | Scott K Gilchrist NORTHGATE TECHNOLOGIES, INC. 3930 VENTURA DR. Arlington Heights, IL 60004 |
| Product Code | FFK |
| CFR Regulation Number | 876.4480 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1991-10-09 |
| Decision Date | 1992-01-06 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00817183020578 | K914514 | 000 |
| 00817183020516 | K914514 | 000 |
| 00817183020509 | K914514 | 000 |
| 10817183020162 | K914514 | 000 |
| 00817183020158 | K914514 | 000 |
| 00817183020141 | K914514 | 000 |
| 00817183020134 | K914514 | 000 |