FETAL HEART DETECTOR #D206— 510(k) K800859
Substantially EquivalentSonicaid, Inc.
FDA 510(k) clearance K800859 for FETAL HEART DETECTOR #D206, Substantially Equivalent on 1980-05-14. Applicant: Sonicaid, Inc.. Device class: 2.
Clearance details
- Applicant
- Sonicaid, Inc.
- 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
- Traditional
- Location
- Mchenry, IL, US
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