Vitrolife AB/Scandinavian Ivf Sciences AB
Washington, DC, US
Vitrolife AB/Scandinavian Ivf Sciences AB appears in FDA device records in Washington, DC. FDA records list 7 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.
FDA records held for this company
- 510(k) clearances
- 7
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 7 510(k) clearances for Vitrolife AB/Scandinavian Ivf Sciences AB in 2000.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 2000 | 7 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K000619 | SCANDINAVIAN IVF SCIENCES AB, G2.2 | MQL | Substantially Equivalent | |
| K000627 | SCANDINAVIAN IVF SCIENCES AB, HYBASE-1 | MQL | Substantially Equivalent | |
| K000626 | SCANDINAVIAN IVF SCIENCES AB, GAMETE-100 | MQL | Substantially Equivalent | |
| K000625 | SCANDINAVIAN IVF SCIENCES AB, G1.2 | MQL | Substantially Equivalent | |
| K000618 | SCANDINAVIAN IVF SCIENCES AB, THAW-KIT 1 | MQL | Substantially Equivalent | |
| K000623 | SCANDINAVIAN IVF SCIENCES AB, FREEZE-KIT 1 | MQL | Substantially Equivalent | |
| K000621 | SCANDINAVIAN IVF SCIENCES AB, SPERMRINSE -20/100 | MQL | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
Recall records
No recall records for this company in the ingested FDA data.
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain