INSEMI-CATH
FDA 510(k) clearance K931630 · decided 1994-04-19
Clearance details
- K-number
- K931630
- Device name
- INSEMI-CATH
- Applicant
- Cook Ob/Gyn
- Decision
- Substantially Equivalent
- Date received
- 1993-04-02
- Decision date
- 1994-04-19
- Days to decision
- 382 days
- Clearance type
- Traditional
- Product code
- MFD
- Device class
- 2
- Regulation number
- 884.5250
- Medical specialty
- Obstetrics/Gynecology
- Advisory committee
- Obstetrics/Gynecology
- Location
- Spencer, IN, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.