INVIGRA
FDA 510(k) clearance K020223 · decided 2002-03-04
Clearance details
- K-number
- K020223
- Device name
- INVIGRA
- Applicant
- Indus Medicare , Ltd.
- Decision
- Substantially Equivalent
- Date received
- 2002-01-22
- Decision date
- 2002-03-04
- Days to decision
- 41 days
- Clearance type
- Abbreviated
- Product code
- HIS
- Device class
- 2
- Regulation number
- 884.5300
- Medical specialty
- Obstetrics/Gynecology
- Advisory committee
- Obstetrics/Gynecology
- Location
- Hyderabad Andhra Pradesh, IN
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.