IUI CATHETER, MODEL 9057— 510(k) K052059
Substantially EquivalentInntec, Inc.
FDA 510(k) clearance K052059 for IUI CATHETER, MODEL 9057, Substantially Equivalent on 2005-11-22. Applicant: Inntec, Inc.. Device class: 2.
Clearance details
- Applicant
- Inntec, Inc.
- Product code
- Code MQF
- Device class
- Class 2
- Regulation
- 21 CFR 884.6110
- Advisory panel
- Obstetrics/Gynecology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Abbreviated
- Location
- Stoughton, WI, US
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