VAKUTAGE— 510(k) K823080
Substantially EquivalentWeston, Copco, Inc.
FDA 510(k) clearance K823080 for VAKUTAGE, Substantially Equivalent on 1982-11-24. Applicant: Weston, Copco, Inc.. Device class: 2.
Clearance details
- Applicant
- Weston, Copco, Inc.
- Product code
- Code HHK
- Device class
- Class 2
- Regulation
- 21 CFR 884.1175
- Advisory panel
- Obstetrics/Gynecology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
Recent devices under product code HHK
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