The following data is part of a premarket notification filed by Gyrus Medical Ltd. with the FDA for Plasmakinetic Endourology System.
| Device ID | K003569 |
| 510k Number | K003569 |
| Device Name: | PLASMAKINETIC ENDOUROLOGY SYSTEM |
| Classification | Unit, Electrosurgical, Endoscopic (with Or Without Accessories) |
| Applicant | GYRUS MEDICAL LTD. FORTRAN RD., ST. MELLONS Cardiff, GB Cf3 0lt |
| Contact | David Kay |
| Correspondent | David Kay GYRUS MEDICAL LTD. FORTRAN RD., ST. MELLONS Cardiff, GB Cf3 0lt |
| Product Code | KNS |
| CFR Regulation Number | 876.4300 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2000-11-20 |
| Decision Date | 2000-12-19 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00821925009219 | K003569 | 000 |