HANDYDOP— 510(k) K030466
Substantially EquivalentElcat, GmbH
FDA 510(k) clearance K030466 for HANDYDOP, Substantially Equivalent on 2003-09-12. Applicant: Elcat, GmbH. Device class: 2.
Clearance details
- Applicant
- Elcat, GmbH
- Product code
- Code KNG
- Device class
- Class 2
- Regulation
- 21 CFR 884.2660
- Advisory panel
- Obstetrics/Gynecology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Abbreviated
- Location
- Alpharetta, GA, US
Recent devices under product code KNG
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