HUI MINI-FLEX
FDA 510(k) clearance K895659 · decided 1989-12-19
Clearance details
- K-number
- K895659
- Device name
- HUI MINI-FLEX
- Applicant
- Unimar, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1989-09-20
- Decision date
- 1989-12-19
- Days to decision
- 90 days
- Clearance type
- Traditional
- Product code
- HIG
- Device class
- 2
- Regulation number
- 884.1700
- Medical specialty
- Obstetrics/Gynecology
- Advisory committee
- Obstetrics/Gynecology
- Location
- Wilton, CT, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.