DIASONICS TRANSVAGINAL, TV 7.5 MHZ PROBE— 510(k) K864908

Substantially Equivalent

Diasonics, 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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