The following data is part of a premarket notification filed by Vitrolife Sweden Ab with the FDA for G-rinse, Model 10031.
| Device ID | K022295 |
| 510k Number | K022295 |
| Device Name: | G-RINSE, MODEL 10031 |
| Classification | Media, Reproductive |
| Applicant | VITROLIFE SWEDEN AB MOLNDALSVAGEN 30 Gothenburg, SE Se-412 63 |
| Contact | Eiler Anderson |
| Correspondent | Eiler Anderson VITROLIFE SWEDEN AB MOLNDALSVAGEN 30 Gothenburg, SE Se-412 63 |
| Product Code | MQL |
| CFR Regulation Number | 884.6180 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2002-07-16 |
| Decision Date | 2002-09-12 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 07350025910208 | K022295 | 000 |