InActiv Blue
FDA 510(k) clearance K221547 · decided 2024-06-11
Clearance details
- K-number
- K221547
- Device name
- InActiv Blue
- Applicant
- Fertipro NV
- Decision
- Substantially Equivalent
- Date received
- 2022-05-27
- Decision date
- 2024-06-11
- Days to decision
- 746 days
- Clearance type
- Traditional
- Product code
- QBD
- Device class
- 2
- Regulation number
- 866.2950
- Medical specialty
- Microbiology
- Advisory committee
- Microbiology
- Location
- Beernem, BE
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.