CR SPIRAL ELECTRODE— 510(k) K910815
Substantially EquivalentNeward Enterprises, Inc.
FDA 510(k) clearance K910815 for CR SPIRAL ELECTRODE, Substantially Equivalent on 1991-12-10. Applicant: Neward Enterprises, Inc.. Device class: 2.
Clearance details
- Applicant
- Neward Enterprises, Inc.
- Product code
- Code HGP
- Device class
- Class 2
- Regulation
- 21 CFR 884.2675
- Advisory panel
- Obstetrics/Gynecology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Cucamonga, CA, US
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