COOPERSURGICAL OOCYTE RECOVERY NEEDLES— 510(k) K023930
Substantially EquivalentCooperSurgical, Inc.
FDA 510(k) clearance K023930 for COOPERSURGICAL OOCYTE RECOVERY NEEDLES, Substantially Equivalent on 2003-01-22. Applicant: CooperSurgical, Inc.. Device class: 2.
Clearance details
- Applicant
- CooperSurgical, Inc.
- Product code
- Code MQE
- Device class
- Class 2
- Regulation
- 21 CFR 884.6100
- Advisory panel
- Obstetrics/Gynecology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Huntington, CT, US
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More clearances from CooperSurgical, Inc.
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