The following data is part of a premarket notification filed by Kinetic Medical Products with the FDA for Microsurgical Cystotome.
| Device ID | K890218 |
| 510k Number | K890218 |
| Device Name: | MICROSURGICAL CYSTOTOME |
| Classification | Surgical Instruments, G-u, Manual (and Accessories) |
| Applicant | KINETIC MEDICAL PRODUCTS 4934 PEACH ST. Erie, PA 16509 |
| Contact | James I Laughner |
| Correspondent | James I Laughner KINETIC MEDICAL PRODUCTS 4934 PEACH ST. Erie, PA 16509 |
| Product Code | KOA |
| CFR Regulation Number | 876.4730 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1989-01-18 |
| Decision Date | 1989-01-27 |