The following data is part of a premarket notification filed by Hologic, Inc. with the FDA for Myosure Xl Rod Lens Hysteroscope, Myosure Xl Outlfow Channel.
| Device ID | K122563 |
| 510k Number | K122563 |
| Device Name: | MYOSURE XL ROD LENS HYSTEROSCOPE, MYOSURE XL OUTLFOW CHANNEL |
| Classification | Hysteroscope (and Accessories) |
| Applicant | HOLOGIC, INC. 250 CAMPUS DRIVE Marlborough, MA 01752 |
| Contact | Sarah Fairfield |
| Correspondent | Sarah Fairfield HOLOGIC, INC. 250 CAMPUS DRIVE Marlborough, MA 01752 |
| Product Code | HIH |
| CFR Regulation Number | 884.1690 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2012-08-22 |
| Decision Date | 2012-09-19 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 25420045510330 | K122563 | 000 |
| 15420045510333 | K122563 | 000 |
| 15420045510234 | K122563 | 000 |
| 15420045510227 | K122563 | 000 |