DIASONICS TRANSVAGINAL, TV 7.5 MHZ PROBE— 510(k) K864908
Substantially EquivalentDiasonics, Inc.
FDA 510(k) clearance K864908 for DIASONICS TRANSVAGINAL, TV 7.5 MHZ PROBE, Substantially Equivalent on 1987-03-27. Applicant: Diasonics, Inc.. Device class: 2.
Clearance details
- Applicant
- Diasonics, Inc.
- Product code
- Code HGL
- Device class
- Class 2
- Regulation
- 21 CFR 884.2960
- Advisory panel
- Obstetrics/Gynecology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Milipitas, CA, US
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