FETAL DOPPLER— 510(k) K905536

Name: FDA 510(k) clearance K905536
Creator: U.S. Food and Drug Administration
Published: 1992-04-21

Substantially Equivalent

Toshiba America Medical Systems, In.C

FDA 510(k) clearance K905536 for FETAL DOPPLER, Substantially Equivalent on 1992-04-21. Applicant: Toshiba America Medical Systems, In.C. Device class: 2.

Clearance details

Applicant: Toshiba America Medical Systems, In.C
Product code: Code MAA
Device class: Class 2
Regulation: 21 CFR 884.2660
Advisory panel: Obstetrics/Gynecology
Date received: 1990-12-11
Decision date: 1992-04-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Tustin, CA, US

Download summary PDF View on FDA.gov ↗

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