The following data is part of a premarket notification filed by Smith & Nephew, Inc. with the FDA for Truclear Incisor Plus Blade 2.9.
| Device ID | K103389 |
| 510k Number | K103389 |
| Device Name: | TRUCLEAR INCISOR PLUS BLADE 2.9 |
| Classification | Hysteroscope (and Accessories) |
| Applicant | SMITH & NEPHEW, INC. 150 MINUTEMAN RD. Andover, MA 01810 |
| Contact | Janice Haselton |
| Correspondent | Janice Haselton SMITH & NEPHEW, INC. 150 MINUTEMAN RD. Andover, MA 01810 |
| Product Code | HIH |
| CFR Regulation Number | 884.1690 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2010-11-18 |
| Decision Date | 2011-03-25 |
| Summary: | summary |